Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants (2020)
Source: Journal of clinical endocrinology & metabolism. Unidade: FM
Subjects: RADIOGRAFIA, POLIMORFISMO, MUTAÇÃO, MÃO, ESTUDOS DE COORTES, CRIANÇAS
ABNT
SENTCHORDI-MONTANE, Lucia et al. Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants. Journal of clinical endocrinology & metabolism, v. 105, n. 8, p. 2654-2666, 2020Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgaa218. Acesso em: 10 fev. 2026.APA
Sentchordi-Montane, L., Benito-Sanz, S., Aza-Carmona, M., Pereda, A., Parron-Pajares, M., Torre, C. de la, et al. (2020). Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants. Journal of clinical endocrinology & metabolism, 105( 8), 2654-2666. doi:10.1210/clinem/dgaa218NLM
Sentchordi-Montane L, Benito-Sanz S, Aza-Carmona M, Pereda A, Parron-Pajares M, Torre C de la, Vasques GA, Funari MFA, Travessa AM, Jorge AA de L. Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants [Internet]. Journal of clinical endocrinology & metabolism. 2020 ; 105( 8): 2654-2666.[citado 2026 fev. 10 ] Available from: https://doi.org/10.1210/clinem/dgaa218Vancouver
Sentchordi-Montane L, Benito-Sanz S, Aza-Carmona M, Pereda A, Parron-Pajares M, Torre C de la, Vasques GA, Funari MFA, Travessa AM, Jorge AA de L. Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants [Internet]. Journal of clinical endocrinology & metabolism. 2020 ; 105( 8): 2654-2666.[citado 2026 fev. 10 ] Available from: https://doi.org/10.1210/clinem/dgaa218
