Atypical presentation of SLC30A10 gene mutation with hypermanganesemia, seizures and polycythemia

por Jagadish, Spoorthi, Howard, Lillian, Thati Ganganna, Sreenath
Publicado 2021

Description of familial keloids in five pedigrees: evidence for autosomal dominant inheritance and phenotypic heterogeneity

por Clark, Jason A, Turner, Maria L, Howard, Lillian, Stanescu, Horia, Kleta, Robert, Kopp, Jeffrey B
Publicado 2009