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Candidate loci chromosome 3 mapped for Santos syndrome (OMIM 613005) (2013)
Alves, L. U; Thiele-Aguiar, Renata Soares; Santos, S; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Resumos. Conference titles: Congresso Brasileiro de Genética. Unidade: IB
Subjects: MALFORMAÇÕES, HERANÇA GENÉTICA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, L. U et al. Candidate loci chromosome 3 mapped for Santos syndrome (OMIM 613005). 2013, Anais.. Águas de Lindóia: Sociedade Brasileira de Genática - SBG, 2013. Disponível em: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf. Acesso em: 17 nov. 2024.
APA
Alves, L. U., Thiele-Aguiar, R. S., Santos, S., Otto, P. A., & Mingroni Netto, R. C. (2013). Candidate loci chromosome 3 mapped for Santos syndrome (OMIM 613005). In Resumos. Águas de Lindóia: Sociedade Brasileira de Genática - SBG. Recuperado de http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
NLM
Alves LU, Thiele-Aguiar RS, Santos S, Otto PA, Mingroni Netto RC. Candidate loci chromosome 3 mapped for Santos syndrome (OMIM 613005) [Internet]. Resumos. 2013 ;[citado 2024 nov. 17 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
Vancouver
Alves LU, Thiele-Aguiar RS, Santos S, Otto PA, Mingroni Netto RC. Candidate loci chromosome 3 mapped for Santos syndrome (OMIM 613005) [Internet]. Resumos. 2013 ;[citado 2024 nov. 17 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
Artigo de periodico
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion (2012)
Klopocki, Eva; Lohan, Silke; Doelken Sandra C; Stricker, Sigmar; Ockeloen, Charlotte W; Aguiar, Renata Soares Thiele de; Lezirovitz, Karina; Mingroni Netto, Regina Celia ; Jamsheer, Aleksander; Shah, Hitesh; Kurth, Ingo; Habenicht, Rolf; Warman, Matthew; Devriendt, Koenraad; Kordaß, Ulrike; Hempel, Maja; Rajab, Anna; Mäkitie, Outi; Naveed, Mohammed; Radhakrishna, Uppala; Antonarakis, Stylianos E
Source: Journal of Medical Genetics. Unidade: IB
Subjects: MALFORMAÇÕES, DOENÇAS GENÉTICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KLOPOCKI, Eva et al. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics, v. 49, n. 2, p. 119-125, 2012Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2011-100409. Acesso em: 17 nov. 2024.
APA
Klopocki, E., Lohan, S., Doelken Sandra C,, Stricker, S., Ockeloen, C. W., Aguiar, R. S. T. de, et al. (2012). Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics, 49( 2), 119-125. doi:10.1136/jmedgenet-2011-100409
NLM
Klopocki E, Lohan S, Doelken Sandra C, Stricker S, Ockeloen CW, Aguiar RST de, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordaß U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 119-125.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100409
Vancouver
Klopocki E, Lohan S, Doelken Sandra C, Stricker S, Ockeloen CW, Aguiar RST de, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordaß U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 119-125.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100409
Artigo de periodico
A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 (2008)
Lezirovitz, Karina; Maestrelli, Sylvia Regina Pedrosa; Cotrim, Nelson Henderson; Otto, Paulo A ; Pearson, Peter Lees; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEZIROVITZ, Karina et al. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3. Human Genetics, v. 123, n. 6, p. 625-631, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00439-008-0515-7. Acesso em: 17 nov. 2024.
APA
Lezirovitz, K., Maestrelli, S. R. P., Cotrim, N. H., Otto, P. A., Pearson, P. L., & Mingroni Netto, R. C. (2008). A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3. Human Genetics, 123( 6), 625-631. doi:10.1007/s00439-008-0515-7
NLM
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 [Internet]. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00439-008-0515-7
Vancouver
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 [Internet]. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00439-008-0515-7

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