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Artigo de periodico
Ring-shaped skin creases syndrome: report of a brazilian family (1998)
Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Zechi, Roseli Maria
Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC
Subjects: GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e NAKATA, Nancy Mizue Kokitsu e ZECHI, Roseli Maria. Ring-shaped skin creases syndrome: report of a brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 1, n. Ja 1998, p. 13-18, 1998Tradução . . Acesso em: 03 jun. 2024.
APA
Guion-Almeida, M. L., Nakata, N. M. K., & Zechi, R. M. (1998). Ring-shaped skin creases syndrome: report of a brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 1( Ja 1998), 13-18.
NLM
Guion-Almeida ML, Nakata NMK, Zechi RM. Ring-shaped skin creases syndrome: report of a brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( Ja 1998): 13-18.[citado 2024 jun. 03 ]
Vancouver
Guion-Almeida ML, Nakata NMK, Zechi RM. Ring-shaped skin creases syndrome: report of a brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( Ja 1998): 13-18.[citado 2024 jun. 03 ]
Artigo de periodico
Smith-Fineman-Myers syndrome in apparently monozygotic twins (1998)
Guion-Almeida, Maria Leine; Tabith Junior, Alfredo; Nakata, Nancy Mizue Kokitsu; Zechi, Roseli Maria
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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 . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980923)79:3%3C205::aid-ajmg11%3E3.0.co;2-l. Acesso em: 03 jun. 2024.
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 [Internet]. American Journal of Medical Genetics. 1998 ; 79( 3): 205-208.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980923)79:3%3C205::aid-ajmg11%3E3.0.co;2-l
Vancouver
Guion-Almeida ML, Tabith Junior A, Nakata NMK, Zechi RM. Smith-Fineman-Myers syndrome in apparently monozygotic twins [Internet]. American Journal of Medical Genetics. 1998 ; 79( 3): 205-208.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980923)79:3%3C205::aid-ajmg11%3E3.0.co;2-l
Artigo de periodico
Brief clinical report: autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial limb anomalies and clubfeet report of a patient with polydactyly of the halluces (1998)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC
Subjects: GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Brief clinical report: autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial limb anomalies and clubfeet report of a patient with polydactyly of the halluces. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 2, n. 1, p. 27-30, 1998Tradução . . Acesso em: 03 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1998). Brief clinical report: autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial limb anomalies and clubfeet report of a patient with polydactyly of the halluces. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 2( 1), 27-30.
NLM
Guion-Almeida ML, Richieri-Costa A. Brief clinical report: autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial limb anomalies and clubfeet report of a patient with polydactyly of the halluces. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 2( 1): 27-30.[citado 2024 jun. 03 ]
Vancouver
Guion-Almeida ML, Richieri-Costa A. Brief clinical report: autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial limb anomalies and clubfeet report of a patient with polydactyly of the halluces. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 2( 1): 27-30.[citado 2024 jun. 03 ]
Artigo de periodico
Say syndrome a new Brazilian case (1998)
Guion-Almeida, Maria Leine; Zechi, Roseli Maria; Nakata, Nancy Mizue Kokitsu
Source: Genetics and Molecular Biology. Unidade: HRAC
Subjects: GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e ZECHI, Roseli Maria e NAKATA, Nancy Mizue Kokitsu. Say syndrome a new Brazilian case. Genetics and Molecular Biology, v. 21, n. 4, p. 449-451, 1998Tradução . . Disponível em: https://doi.org/10.1590/s1415-47571998000400007. Acesso em: 03 jun. 2024.
APA
Guion-Almeida, M. L., Zechi, R. M., & Nakata, N. M. K. (1998). Say syndrome a new Brazilian case. Genetics and Molecular Biology, 21( 4), 449-451. doi:10.1590/s1415-47571998000400007
NLM
Guion-Almeida ML, Zechi RM, Nakata NMK. Say syndrome a new Brazilian case [Internet]. Genetics and Molecular Biology. 1998 ; 21( 4): 449-451.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1590/s1415-47571998000400007
Vancouver
Guion-Almeida ML, Zechi RM, Nakata NMK. Say syndrome a new Brazilian case [Internet]. Genetics and Molecular Biology. 1998 ; 21( 4): 449-451.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1590/s1415-47571998000400007
Artigo de periodico
Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients (1998)
Guion-Almeida, Maria Leine; Rodini, Elaine S. Oliveira; Nakata, Nancy Mizue Kokitsu; Amantini, Denise Bologna
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients. American Journal of Medical Genetics, v. 76, n. 5, p. 133-136, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u. Acesso em: 03 jun. 2024.
APA
Guion-Almeida, M. L., Rodini, E. S. O., Nakata, N. M. K., & Amantini, D. B. (1998). Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients. American Journal of Medical Genetics, 76( 5), 133-136. doi:10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u
NLM
Guion-Almeida ML, Rodini ESO, Nakata NMK, Amantini DB. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients [Internet]. American Journal of Medical Genetics. 1998 ; 76( 5): 133-136.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u
Vancouver
Guion-Almeida ML, Rodini ESO, Nakata NMK, Amantini DB. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients [Internet]. American Journal of Medical Genetics. 1998 ; 76( 5): 133-136.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u

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