Inter- and Intrachromosomal Rearrangements Are Both Involved in the Origin of 15q11-q13 Deletions in Prader-Willi Syndrome-Reference-Cited by-同舟云学术

Inter- and Intrachromosomal Rearrangements Are Both Involved in the Origin of 15q11-q13 Deletions in Prader-Willi Syndrome

Published:1997-07 Issue:1 Volume:61 Page:228-231
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Carrozzo Romeo,Rossi Elena,Christian Susan L.,Kittikamron Kirk,Livieri Chiara,Corrias Andrea,Pucci Lucia,Fois Alberto,Bosio Laura,Simi Paolo,Beccaria Luciano,Zuffardi Orsetta,Ledbetter David H.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17;Chance;Hum Mol Genet,1994

2. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients;Christian;Am J Hum Genet,1995

3. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome;Clayton-Smith;J Med Genet,1993

4. Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome;Dutly;Hum Mol Genet,1996

5. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes;Huang;Hum Genet,1997

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