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For: Sentchordi-Montané L, Benito-Sanz S, Aza-Carmona M, Pereda A, Parrón-Pajares M, de la Torre C, Vasques GA, Funari MFA, Travessa AM, Dias P, Suarez-Ortega L, González-Buitrago J, Portillo-Najera NE, Llano-Rivas I, Martín-Frías M, Ramírez-Fernández J, Sánchez Del Pozo J, Garzón-Lorenzo L, Martos-Moreno GA, Alfaro-Iznaola C, Mulero-Collantes I, Ruiz-Ocaña P, Casano-Sancho P, Portela A, Ruiz-Pérez L, Del Pozo A, Vallespín E, Solís M, Lerario AM, González-Casado I, Ros-Pérez P, Pérez de Nanclares G, Jorge AAL, Heath KE. Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants. J Clin Endocrinol Metab 2020;105:dgaa218. [PMID: 32311039 DOI: 10.1210/clinem/dgaa218] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Baz-redón N, Soler-colomer L, Fernández-cancio M, Benito-sanz S, Garrido M, Moliné T, Clemente M, Camats-tarruella N, Yeste D. Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report. Front Endocrinol 2022;13:957969. [DOI: 10.3389/fendo.2022.957969] [Reference Citation Analysis]
2 Li X, Yang S, Chinipardaz Z, Koyama E, Yang S. SAG therapy restores bone growth and reduces enchondroma incidence in a model of skeletal chondrodysplasias caused by Ihh deficiency. Mol Ther Methods Clin Dev 2021;23:461-75. [PMID: 34820473 DOI: 10.1016/j.omtm.2021.09.015] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 de Brito Chagas J, Cordinhã C, do Carmo C, Alves C, Heath KE, Sousa SB, Gomes C. Vitamin D-Dependent Rickets Type 1A in Two Siblings with a Hypomorphic CYP27B1 Variant Frequent in the African Population. J Pediatr Genet. [DOI: 10.1055/s-0041-1736559] [Reference Citation Analysis]
4 Onuki T, Shibata N, Hiroshima S, Sawano K, Nagasaki K. A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings. Congenit Anom (Kyoto) 2021. [PMID: 34591992 DOI: 10.1111/cga.12445] [Reference Citation Analysis]
5 Ozyavuz Cubuk P, Duz MB. Acrocapitofemoral dysplasia: Novel mutation in IHH in two adult patients from the third family in the literature and progression of the disease. Eur J Med Genet 2021;64:104343. [PMID: 34530144 DOI: 10.1016/j.ejmg.2021.104343] [Reference Citation Analysis]
6 Costantini A, Muurinen MH, Mäkitie O. New gene discoveries in skeletal diseases with short stature. Endocr Connect 2021;10:R160-74. [PMID: 33830070 DOI: 10.1530/EC-21-0083] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]