Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”)-Reference-Cited by-同舟云学术

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Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”)

Published:2002-04 Issue:4 Volume:70 Page:866-874
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Brouillard Pascal,Boon Laurence M.,Mulliken John B.,Enjolras Odile,Ghassibé Michella,Warman Matthew L.,Tan O.T.,Olsen Bjorn R.,Vikkula Miikka

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. A gene for inherited cutaneous venous anomalies (“glomangiomas”) localizes to chromosome 1p21-22;Boon;Am J Hum Genet,1999

2. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p;Boon;Hum Mol Genet,1994

3. High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22;Brouillard;Genomics,2000

4. Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity;Calvert;Hum Hered,2001

5. Allelic and locus heterogeneity in inherited venous malformations;Calvert;Hum Mol Genet,1999

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