Source: European journal of endocrinology. Unidade: FM
Subjects: GENES HOMEOBOX, DIVERSIDADE GENÉTICA, NANISMO
ABNT
DANTAS, Naiara Castelo Branco et al. Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability. European journal of endocrinology, v. 189, n. 3, p. 387-395, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57310. Acesso em: 04 set. 2024.APA
Dantas, N. C. B., Funari, M. F. de A., Lerario, A. M., Andrade, N. L. M., Rezende, R. C., Cellin, L. de P., et al. (2023). Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability. European journal of endocrinology, 189( 3), 387-395. doi:10.1093/ejendo/lvad128NLM
Dantas NCB, Funari MF de A, Lerario AM, Andrade NLM, Rezende RC, Cellin L de P, Alves C, Crisóstomo LG, Arnhold IJP, Mendonca BB de, Scalco R da C, Jorge AA de L. Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability [Internet]. European journal of endocrinology. 2023 ; 189( 3): 387-395.[citado 2024 set. 04 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57310Vancouver
Dantas NCB, Funari MF de A, Lerario AM, Andrade NLM, Rezende RC, Cellin L de P, Alves C, Crisóstomo LG, Arnhold IJP, Mendonca BB de, Scalco R da C, Jorge AA de L. Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability [Internet]. European journal of endocrinology. 2023 ; 189( 3): 387-395.[citado 2024 set. 04 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57310