Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)-Reference-Cited by-同舟云学术

Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)

Published:2010-03 Issue:3 Volume:86 Page:471-478
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Meyer Esther,Ricketts Christopher,Morgan Neil V.,Morris Mark R.,Pasha Shanaz,Tee Louise J.,Rahman Fatimah,Bazin Anne,Bessières Bettina,Déchelotte Pierre,Yacoubi Mohamed T.,Al-Adnani Mudher,Marton Tamas,Tannahill David,Trembath Richard C.,Fallet-Bianco Catherine,Cox Phillip,Williams Denise,Maher Eamonn R.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference30 articles.

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3. Fetal neuropathology of proliferative vasculopathy and hydranencephaly-hydrocephaly with multiple limb pterygia;Norman;Pediatr. Neurosci.,1988

4. The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferation;Harding;Neuropathol. Appl. Neurobiol.,1995

5. Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction;Castro-Gago;J. Child Neurol.,2001

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