WorldCat Link Resolver, the OpenURL link-server from OCLC

Mutation analysis of MECP2 and determination of the X-inacti…

Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients.

Article, Chapter

Authors: J. Karteszi

Publication: American Journal of Medical Genetics Part A, Volume:131, Issue:1, Page(s):106

Published: Wiley, 2004

ISSN: 1552-4825

Full text availability for this item

View Full Text Source:American Journal of Medical Genetics Part A,American Journal of Medical Genetics Part A,Wiley Online Library Database Model 2021 Opens in new Window

Journal: American Journal of Medical Genetics Part A Source:Wiley Online Library Database Model 2021 Opens in new Window

Collection: Wiley Online Library Database Model 2021 Opens in new Window

Coverage:

2003~present; ;issue:1~present

View Full Text Source:American Journal of Medical Genetics Part A,American Journal of Medical Genetics Part A,Wiley Online Library: Complete Journals Opens in new Window

Journal: American Journal of Medical Genetics Part A Source:Wiley Online Library: Complete Journals Opens in new Window

Collection: Wiley Online Library: Complete Journals Opens in new Window

Coverage:

2003-01-01~present; ;issue:1~present

Browse related articles

Print copies at your library

Check availability in RUQuest

Request a copy of this item

Cite this item