Brasil | Article

Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia

Fecha
2018
Registro en:
GOMES, Maria E. S. et al. Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia. Molecular Syndromology, p. 1-8, 2018.
1661-8769
10.1159/000486697
Autor
Gomes, Maria E. S.
Kanazawa, Thatiane Y.
Riba, Fernanda R.
Pereira, Natálya Gonçalves
Zuma, Maria C. C.
Rabelo, Natana C.
Sanseverino, Maria T.
Horovitz, Dafne Dain Gandelman
Llerena Junior, Juan Clinton
Cavalcanti, Denise P.
Gonzalez, Sayonara
Institución
Materias

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