Infantile hydrocephalus: A review of epidemiology, classification and causes-Reference-Cited by-同舟云学术

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Infantile hydrocephalus: A review of epidemiology, classification and causes

Published:2014-08 Issue:8 Volume:57 Page:359-368
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Tully Hannah M.,Dobyns William B.

Funder

National Center for Advancing Translational Sciences of the National Institutes of Health

National Institute of Neurological Disorders and Stroke of the National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference97 articles.

1. Similar and distinct properties of MUPP1 and Patj, two homologous PDZ domain-containing tight-junction proteins;Adachi;Mol Cell Biol,2009

2. Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases;Adle-Biassette;Acta Neuropathol,2013

3. Mutation in MPDZ causes severe congenital hydrocephalus;Al-Dosari;J Med Genet,2013

4. Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa;Ali;Investigative Ophthalmol Vis Sci,2011

5. Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis;Allache;Birth Defects Res A Clin Mol Teratol,2012

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