Molecular definition of the Prader — Willi syndrome chromosome region and orientation of the SNRPN gene-Reference-Cited by-同舟云学术

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Molecular definition of the Prader — Willi syndrome chromosome region and orientation of the SNRPN gene

Published:1993 Issue:12 Volume:2 Page:1991-1994
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Bulting Karin,Dlttrich Bärbel,Groß Stephanle,Greger Valerle,Lalande Marc,Robinson Wendy,Mutirangura Apiwat,Ledbetter David,Horsthemke Bernhard

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/2/12/1991/1828892/2-12-1991.pdf

Cited by 29 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. The adult phenotype of Schaaf-Yang syndrome;Orphanet Journal of Rare Diseases;2020-10-19

2. The imprinted NPAP1/C15orf2 gene in the Prader–Willi syndrome region encodes a nuclear pore complex associated protein;Human Molecular Genetics;2012-06-13

3. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome;European Journal of Human Genetics;2008-12-10

4. A 15-Year-Old With Drop Attacks and Unsteadiness While Descending Stairs;Seminars in Pediatric Neurology;2008-12

5. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?;Clinical Genetics;2008-10-09

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