Proximal duplications of chromosome 15: clinical dilemmas

Author:

Hood O. J.,Rouse Bobbye M.,Lockhart L. H.,Bodensteiner J. B.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Familial partial trisomy 15: identification of a deleted no. 15 confirmed by anti-5-methylcyto-dine antibody binding;Breg;Am. J. Hum. Genet.,1974

2. A case of trisomy of chromosome 15;Coldwell;J. Med. Genet.,1981

3. Three cases of partial tetrasomy 15;Falco;Am. J. Hum. Genet.,1978

4. Deficiency transposition, and duplication of one 15q region may be alternat-tively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment;Fraccaro;Hum. Genet.,1983

5. Location of ribosomal DNA in the human chromosome complement;Henderson;Proc. Natl. Acad. Sci. USA,1972

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2. Disorders of Brain Size;Swaiman's Pediatric Neurology;2012

3. The evaluation of 15q proximal duplications by FISH;Clinical Genetics;2008-06-28

4. De novo paracentric inversion (X)(q26q28) with features mimicking Prader-Willi syndrome;American Journal of Medical Genetics;2003-07-30

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