Congenital nephropathy and ventriculomegaly: a report of four cases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference8 articles.
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2. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome
3. Risks for Fetal Abnormalities after very and moderately elevated AF-AFPs
4. Nephrin Localizes at the Podocyte Filtration Slit Area and Is Characteristically Spliced in the Human Kidney
5. Defect of cerebellar Purkinje cell histogenesis associated with type I and type II renal cystic disease
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Expansion of phenotype and genotypic data in CRB2-related syndrome;European Journal of Human Genetics;2016-03-23
2. CRB2 Mutations Produce a Phenotype Resembling Congenital Nephrosis, Finnish Type, with Cerebral Ventriculomegaly and Raised Alpha-Fetoprotein;The American Journal of Human Genetics;2015-01
3. Update on congenital nephrotic syndromes and the contribution of US;Pediatric Radiology;2010-08-17
4. N;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
5. Maternal serum alpha-fetoprotein levels in fetal hydrocephalus: a retrospective population based study;BMC Pregnancy and Childbirth;2006-07-07
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