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Autor:
Maria E S, Gomes, Thatiane Y, Kanazawa, Fernanda R, Riba, Natálya G, Pereira, Maria C C, Zuma, Natana C, Rabelo, Maria T, Sanseverino, Dafne D G, Horovitz, Juan C, Llerena, Denise P, Cavalcanti, Sayonara, Gonzalez
Publikováno v:
Molecular syndromology. 9(2)
Mutations in the fibroblast growth factor receptor 3 gene (FGFR3) cause achondroplasia (ACH), hypochondroplasia (HCH), and thanatophoric dysplasia types I and II (TDI/TDII). In this study, we performed a genetic study of 123 Brazilian patients with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c96d616feea1bfb55a1e78372f9828c
https://pubmed.ncbi.nlm.nih.gov/29593476
https://pubmed.ncbi.nlm.nih.gov/29593476
