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Artigo de periodico
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome (2010)
Mazzeu, J F; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Oudakker, A; Rosenberg, Carla ; Szuhai, K; McGill, J; MacCrauhhan, J; Bokhoven, H van; Brunner, H G
Source: Clinical Genetics. Unidade: IB
Subjects: GENÉTICA, DOENÇAS GENÉTICAS
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ABNT
MAZZEU, J F et al. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics, v. 77 n. 4, p. 404-407, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2009.01355.x. Acesso em: 10 out. 2024.
APA
Mazzeu, J. F., Vianna-Morgante, A. M., Krepischi, A. C. V., Oudakker, A., Rosenberg, C., Szuhai, K., et al. (2010). Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics, 77 n. 4, 404-407. doi:10.1111/j.1399-0004.2009.01355.x
NLM
Mazzeu JF, Vianna-Morgante AM, Krepischi ACV, Oudakker A, Rosenberg C, Szuhai K, McGill J, MacCrauhhan J, Bokhoven H van, Brunner HG. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome [Internet]. Clinical Genetics. 2010 ; 77 n. 4 404-407.[citado 2024 out. 10 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01355.x
Vancouver
Mazzeu JF, Vianna-Morgante AM, Krepischi ACV, Oudakker A, Rosenberg C, Szuhai K, McGill J, MacCrauhhan J, Bokhoven H van, Brunner HG. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome [Internet]. Clinical Genetics. 2010 ; 77 n. 4 404-407.[citado 2024 out. 10 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01355.x
Trabalho de evento-resumo
Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
Themmen, A P N; Kraais, R; Kremer, H; Post, M; Toledo, S. P. A.; Brunner, H G; Grootegoed, J A
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
THEMMEN, A P N et al. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 10 out. 2024.
APA
Themmen, A. P. N., Kraais, R., Kremer, H., Post, M., Toledo, S. P. A., Brunner, H. G., & Grootegoed, J. A. (1995). Missense mutation in the lh receptor gene causas leydig cell hypoplasia. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 out. 10 ]
Vancouver
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 out. 10 ]
Artigo de periodico
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene (1995)
Kremer, H; Kraaij, R; Toledo, S. P. A.; Post, M; Fridman, J B; Hayashida, C Y; Reen, M; Milgrom, E.; Ropers, H H; Mariman, E; Themmen, A P N; Brunner, H G
Source: Nature Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREMER, H et al. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, v. 9 , p. 160-4, 1995Tradução . . Disponível em: https://doi.org/10.1038/ng0295-160. Acesso em: 10 out. 2024.
APA
Kremer, H., Kraaij, R., Toledo, S. P. A., Post, M., Fridman, J. B., Hayashida, C. Y., et al. (1995). Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, 9 , 160-4. doi:10.1038/ng0295-160
NLM
Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 out. 10 ] Available from: https://doi.org/10.1038/ng0295-160
Vancouver
Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 out. 10 ] Available from: https://doi.org/10.1038/ng0295-160

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