Clinical and cytogenetic studies of the Prader-Willi syndrome: Evidence of phenotype-karyotype correlation-Reference-Cited by-同舟云学术

Clinical and cytogenetic studies of the Prader-Willi syndrome: Evidence of phenotype-karyotype correlation

Published:1985-01 Issue:1 Volume:69 Page:22-27
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Niikawa N.,Ishikiriyama S.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00295524.pdf

Reference18 articles.

1. Berg R, Engels WR, Kreber RA (1980) Site-specific X-chromosome rearrangements from hybrid dysgenesis in Drosophila melanogaster. Science 210:427?429

2. B�hler EM (1983) Unmasking of heterozygosity by inherited balanced translocations. Implications for prenatal diagnosis and gene mapping. Ann Genet (Paris) 26:133?137

3. Butler MG, Palmer CG (1983) Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet I: 1285?1286

4. Chamberlin J, Magenis RE (1980) Parental origin of de novo chromosome rearrangements. Hum Genet 53:343?347

5. Charrow J, Balkin N, Cohen MM (1983) Translocations in Prader-Willi syndrome. Clin Genet 23:304?307

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