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

Autor: Gomes, Maria E.S., Kanazawa, Thatiane Y., Riba, Fernanda R., Pereira, Natálya G., Zuma, Maria C.C., Rabelo, Natana C., Sanseverino, Maria T., Horovitz, Dafne D.G., Llerena Jr., Juan C., Cavalcanti, Denise P., Gonzalez, Sayonara
Zdroj: Molecular Syndromology; Feb2018, Vol. 9 Issue 2, p92-99, 8p
Databáze: Complementary Index
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