An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3

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An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

Published:1995 Issue:10 Volume:4 Page:1821-1827
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Ferrero Glovanni B.,Franco Brunella,Roth E.Jill,Firulli Beth A.,Borsanl Gluseppe,Delmas-Mata Juan,Weissenbach Jean,Halley George,Schlessinger David,Chinault A.Craig,Y.Zoghbi Huda,L.Nelson David,Ballabio Andrea

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/4/10/1821/2204326/4-10-1821.pdf

Cited by 74 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardation;Clinical Genetics;2008-06-28

2. Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers;American Journal of Medical Genetics Part A;2006

3. A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD;American Journal of Medical Genetics;2003-08-29

4. Gene dosage of the spermidine/spermine N1-acetyltransferase (SSAT) gene with putrescine accumulation in a patient with a Xp21.1p22.12 duplication and keratosis follicularis spinulosa decalvans (KFSD);Human Genetics;2002-08-01

5. Effective Retrovirus-Mediated Gene Transfer in Normal and Mutant Human Melanocytes;Human Gene Therapy;2002-05-20

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