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Mostrando ítems 1-10 de 23
The Novel WT1 Gene Mutation p.H377N Associated to Denys-Drash Syndrome
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2010)
Estudo clínico, molecular e citogenético de tumores embrionários (Neuroblastoma, Tumor de Wilms, Retinoblastoma, Meduloblastoma)
(Universidade Federal de Pernambuco, 2015)
Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria
(Academic Press Inc Elsevier ScienceSan DiegoEUA, 2013)
Nphs2 Mutations Account For Only 15 % Of Nephrotic Syndrome Cases
(BIOMED CENTRAL LTDLONDON, 2015)
FISH studies in a girl with sporadic aniridia and an apparently balanced de novo t(11; 13)(p13; q33) translocation detect a microdeletion involving the WAGR region
(2000)
O estudo citogenético convencional em uma menina com aniridia esporádica resultou em uma aparente translocação balanceada
t(11;13)(p13;q33) de novo. Entretanto, o estudo citogenético pela hibridação in situ fluorescente ...
Clinical and genetic findings of five patients with WT1-related disordersAchados clínicos e genéticos de cinco pacientes com anomalias relacionadas ao gene WT1
(Sociedade Brasileira de Endocrinologia e Metabologia, 2008)
Nphs2 Mutations Account For Only 15% Of Nephrotic Syndrome Cases
(BioMed Central Ltd., 2015)