Maternal origin of deletion 15q11–13 in 25/25 cases of Angelman syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00215668.pdf
Reference12 articles.
1. Angelman H (1965) “Puppet” children: a report on three cases. Dev Med Child Neurol 7:681–683
2. Bloom SE, Goodpasture C (1976) An improved technique for selective silver staining of nucleolar organiser regions in human chromosomes. Hum Genet 34:199–206
3. Butler MG (1990) Prader-Willi syndrome: current understanding of cause and diagnosis. Am J Med Genet 35:319–332
4. Butler MG, Palmer CG (1983) Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet 1:1285–1286
5. Donlon TA (1988) Similar molecular deletions on chromosome 15q11. 2 are encountered in both Prader-Willi and Angelman syndrome. Hum Genet 80:322–328
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4. Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations;The American Journal of Human Genetics;1997-12
5. Diagnosis of Microdeletion Syndromes by Fluorescence in situ Hybridization ( FISH );Current Protocols in Human Genetics;1997-08
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