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Uniparental disomy and gene localization


Schinzel, Albert (1991). Uniparental disomy and gene localization. American Journal of Human Genetics, 48(2):424-425.

Abstract

To the Editor: Uniparental heterodisomy, mentioned as a possible cause of genetic imprinting in the recent review by Hall (1990), has recently been demonstrated to be one possible cause of the Prader-Willi syndrome (Nicholls et al. 1989) and of male-to-male transmission of hemophilie A (Vidaud et al. 1989).

Abstract

To the Editor: Uniparental heterodisomy, mentioned as a possible cause of genetic imprinting in the recent review by Hall (1990), has recently been demonstrated to be one possible cause of the Prader-Willi syndrome (Nicholls et al. 1989) and of male-to-male transmission of hemophilie A (Vidaud et al. 1989).

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Additional indexing

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > Institute of Medical Genetics
Dewey Decimal Classification:570 Life sciences; biology
610 Medicine & health
Scopus Subject Areas:Life Sciences > Genetics
Health Sciences > Genetics (clinical)
Uncontrolled Keywords:Genetics (medical), Genetics, Prader-Willi syndrome
Language:English
Date:February 1991
Deposited On:20 Apr 2023 09:47
Last Modified:29 Apr 2024 01:37
Publisher:Elsevier
ISSN:0002-9297
OA Status:Closed
Free access at:PubMed ID. An embargo period may apply.
PubMed ID:1990849
Other Identification Number:Corpus ID: 87267382