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  • Source: American Journal of Medical Genetics. Unidades: HRAC, HRACF

    Subjects: GENÉTICA, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS

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    • ABNT

      RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 28 set. 2022.
    • APA

      Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305
    • NLM

      Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2022 set. 28 ] Available from: https://doi.org/10.1002/ajmg.a.61305
    • Vancouver

      Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2022 set. 28 ] Available from: https://doi.org/10.1002/ajmg.a.61305
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: NARIZ (ANATOMIA), TOMOGRAFIA COMPUTADORIZADA POR RAIOS X, FENÓTIPOS

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    • ABNT

      GUION-ALMEIDA, Maria Leine e LAMÔNICA NETO, Domingos e LOPES, Vera Lúcia Gil da Silva. Unusual nasal duplication in two patients. American Journal of Medical Genetics, v. No 2004, n. 4, p. 435-436, 2004Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Lamônica Neto, D., & Lopes, V. L. G. da S. (2004). Unusual nasal duplication in two patients. American Journal of Medical Genetics, No 2004( 4), 435-436. doi:10.1002/ajmg.a.30278
    • NLM

      Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: ANORMALIDADES MÚLTIPLAS

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    • ABNT

      GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
    • NLM

      Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: ANORMALIDADES MÚLTIPLAS

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    • ABNT

      NAKATA, Nancy Mizue Kokitsu e GUION-ALMEIDA, Maria Leine. Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics, v. 118A, n. 4, p. 391-393, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Nakata, N. M. K., & Guion-Almeida, M. L. (2003). Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics, 118A( 4), 391-393. doi:10.1002/ajmg.a.10189
    • NLM

      Nakata NMK, Guion-Almeida ML. Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics. 2003 ; 118A( 4): 391-393.[citado 2022 set. 28 ]
    • Vancouver

      Nakata NMK, Guion-Almeida ML. Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics. 2003 ; 118A( 4): 391-393.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, HIPERTELORISMO

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    • ABNT

      PAULA, Ligiane Alves Machado e GUION-ALMEIDA, Maria Leine. Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, v. 117A, n. 2, p. 181-183, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Paula, L. A. M., & Guion-Almeida, M. L. (2003). Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, 117A( 2), 181-183. doi:10.1002/ajmg.a.10919
    • NLM

      Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2022 set. 28 ]
    • Vancouver

      Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: DISOSTOSE CRÂNIOFACIAL

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    • ABNT

      GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, v. 119A, n. 2, p. 238-241, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., & Richieri-Costa, A. (2003). Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, 119A( 2), 238-241. doi:10.1002/ajmg.a.10444
    • NLM

      Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, FISSURA LÁBIOPALATINA, HIPOTIREOIDISMO, ANOMALIA DENTÁRIA

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    • ABNT

      LOPES, Vera Lúcia Gil da Silva e GUION-ALMEIDA, Maria Leine e RODINI, Elaine Sbroggio de Oliveira. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype?. American Journal of Medical Genetics, v. 121A, n. 3, p. 266-270, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Lopes, V. L. G. da S., Guion-Almeida, M. L., & Rodini, E. S. de O. (2003). Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? American Journal of Medical Genetics, 121A( 3), 266-270. doi:10.1002/ajmg.a.20223
    • NLM

      Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2022 set. 28 ]
    • Vancouver

      Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: ANORMALIDADES MÚLTIPLAS

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    • ABNT

      GUION-ALMEIDA, Maria Leine e NAKATA, Nancy Mizue Kokitsu. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics, v. 117, n. 1, p. 84-83, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., & Nakata, N. M. K. (2003). Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics, 117( 1), 84-83.
    • NLM

      Guion-Almeida ML, Nakata NMK. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics. 2003 ; 117( 1): 84-83.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Nakata NMK. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics. 2003 ; 117( 1): 84-83.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: SÍNDROME DE PIERRE ROBIN, ANORMALIDADES CROMOSSÔMICAS

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    • ABNT

      LIMA, Renata Lúcia Leite Ferreira de e MORETTI-FERREIRA, Danilo e RICHIERI-COSTA, Antonio. Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. American Journal of Medical Genetics, v. 122A, n. 1, p. 56-58, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Lima, R. L. L. F. de, Moretti-Ferreira, D., & Richieri-Costa, A. (2003). Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. American Journal of Medical Genetics, 122A( 1), 56-58. doi:10.1002/ajmg.a.20270
    • NLM

      Lima RLLF de, Moretti-Ferreira D, Richieri-Costa A. Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. American Journal of Medical Genetics. 2003 ; 122A( 1): 56-58.[citado 2022 set. 28 ]
    • Vancouver

      Lima RLLF de, Moretti-Ferreira D, Richieri-Costa A. Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. American Journal of Medical Genetics. 2003 ; 122A( 1): 56-58.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: LARINGE, MALFORMAÇÕES, VOZ (FISIOLOGIA), ANORMALIDADES CRANIOFACIAIS

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    • ABNT

      TABITH JUNIOR, Alfredo e GONÇALVES, Cristina Guedes de Azevedo Bento. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, v. 122A, n. 2, p. 133-138, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Tabith Junior, A., & Gonçalves, C. G. de A. B. (2003). Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, 122A( 2), 133-138. doi:10.1002/ajmg.a.10227
    • NLM

      Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2022 set. 28 ]
    • Vancouver

      Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB

    Subject: ANORMALIDADES CRANIOFACIAIS

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    • ABNT

      PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Acesso em: 28 set. 2022.
    • APA

      Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
    • NLM

      Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2022 set. 28 ]
    • Vancouver

      Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: SÍNDROMES OROFACIODIGITAIS

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    • ABNT

      GUION-ALMEIDA, Maria Leine et al. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, v. 112, n. 2, p. 209-214, 2002Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Nakata, N. M. K. (2002). Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, 112( 2), 209-214. doi:10.1002/ajmg.10631
    • NLM

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA MÉDICA

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    • ABNT

      ZANCHETTA, Sthella et al. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, v. No 2000, n. 1, p. 13-16, 2000Tradução . . Acesso em: 28 set. 2022.
    • APA

      Zanchetta, S., Ohara, K., Rodrigues, P. T., Carvalho, E. L. L., & Richieri-Costa, A. (2000). "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, No 2000( 1), 13-16. doi:10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
    • NLM

      Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2022 set. 28 ]
    • Vancouver

      Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA

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    • ABNT

      GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 1, p. 72-77, 1999Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, No 1999( 1), 72-77. doi:10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
    • NLM

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA

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    • ABNT

      CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, v. 86, n. 2, p. 199-201, 1999Tradução . . Acesso em: 28 set. 2022.
    • APA

      Ceide, R. M. Z., & Guion-Almeida, M. L. (1999). Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, 86( 2), 199-201. doi:10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
    • NLM

      Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2022 set. 28 ]
    • Vancouver

      Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA MÉDICA

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    • ABNT

      GUION-ALMEIDA, Maria Leine et al. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, v. 86, n. 2, p. 130-133, 1999Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., & Vendramini, S. (1999). Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, 86( 2), 130-133. doi:10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f
    • NLM

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA

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    • ABNT

      NAKATA, Nancy Mizue Kokitsu e VENDRAMINI, Siulan e GUION-ALMEIDA, Maria Leine. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, v. 86, n. 3, p. 282-284, 1999Tradução . . Acesso em: 28 set. 2022.
    • APA

      Nakata, N. M. K., Vendramini, S., & Guion-Almeida, M. L. (1999). Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, 86( 3), 282-284. doi:10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
    • NLM

      Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2022 set. 28 ]
    • Vancouver

      Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA

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    • ABNT

      GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 3, p. 237-244, 1999Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., & Richieri-Costa, A. (1999). New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, No 1999( 3), 237-244. doi:10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i
    • NLM

      Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidades: IB, HRAC

    Subject: GENÉTICA MÉDICA

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    • ABNT

      PASSOS-BUENO, Maria Rita et al. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, v. 78, p. 237-241, 1998Tradução . . Acesso em: 28 set. 2022.
    • APA

      Passos-Bueno, M. R., Sertié, A. L., Richieri-Costa, A., Alonso, L. G., Zatz, M., Alonso, N., et al. (1998). Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, 78, 237-241. doi:10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
    • NLM

      Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2022 set. 28 ]
    • Vancouver

      Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2022 set. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subject: GENÉTICA

    DOIHow to cite
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    • ABNT

      GUION-ALMEIDA, Maria Leine et al. Smith-Fineman-Myers syndrome in apparently monozygotic twins. American Journal of Medical Genetics, v. 79, n. 3, p. 205-208, 1998Tradução . . Acesso em: 28 set. 2022.
    • APA

      Guion-Almeida, M. L., Tabith Junior, A., Nakata, N. M. K., & Zechi, R. M. (1998). Smith-Fineman-Myers syndrome in apparently monozygotic twins. American Journal of Medical Genetics, 79( 3), 205-208. doi:10.1002/(sici)1096-8628(19980923)79:3%3C205::aid-ajmg11%3E3.0.co;2-l
    • NLM

      Guion-Almeida ML, Tabith Junior A, Nakata NMK, Zechi RM. Smith-Fineman-Myers syndrome in apparently monozygotic twins. American Journal of Medical Genetics. 1998 ; 79( 3): 205-208.[citado 2022 set. 28 ]
    • Vancouver

      Guion-Almeida ML, Tabith Junior A, Nakata NMK, Zechi RM. Smith-Fineman-Myers syndrome in apparently monozygotic twins. American Journal of Medical Genetics. 1998 ; 79( 3): 205-208.[citado 2022 set. 28 ]

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