The male phenotype in osteopathia striata congenita with cranial sclerosis-Reference-Cited by-同舟云学术

The male phenotype in osteopathia striata congenita with cranial sclerosis

Published:2011-08-16 Issue:10 Volume:155 Page:2397-2408
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Holman Sarah K.,Daniel Phil,Jenkins Zandra A.,Herron Rachel L.,Morgan Tim,Savarirayan Ravi,Chow C.W.,Bohring Axel,Mosel Annette,Lacombe Didier,Steiner Bernhard,Schmitt-Mechelke Thomas,Schroter Barbara,Raas-Rothschild Annick,Miñaur Sixto Garcia,Porteous Mary,Parker Michael,Quarrell Oliver,Tapon Dagmar,Cormier-Daire Valérie,Mansour Sahar,Nash Ruth,Bindoff Laurence A.,Fiskerstrand Torunn,Robertson Stephen P.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34178/fullpdf

Reference40 articles.

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2. Osteopathia striata with cranial sclerosis: Literature reappraisal argues for X-linked inheritance;Behninger;Genet Couns,2000

3. Conductive hearing loss in osteopathia striata-cranial sclerosis;Berenholz;Otolaryngol Head Neck Surg,2002

4. Severe malformations in males from families with osteopathia striata with cranial sclerosis;Bueno;Clin Genet,1998

5. Congenital myopathies: Diseases of the actin cytoskeleton;Clarkson;J Pathol,2004

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