Approaches to the prenatal diagnosis of the Prader-Willi syndrome.

Human genetics ·Vol. 74 ·No. 3 ·1986-11-00 ·Pages 327

Schinzel A

Abstract

暂无摘要

MeSH Terms

Chromosome Aberrations/genetics Chromosome Disorders Chromosomes, Human, Pair 15/ultrastructure Female Genetic Counseling Humans Prader-Willi Syndrome/diagnosis,genetics Pregnancy Prenatal Diagnosis

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Schinzel A

References (6)

6 references, click to expand

Cytogenetic studies of familial Prader-Willi syndrome.
Hum Genet. 1984;65(4):325-30 PMID: 6693121
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.
Proc Natl Acad Sci U S A. 1986 Jun;83(12):4408-12 PMID: 3012567
A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.
Hum Genet. 1980;55(2):271-3 PMID: 7450770
Prenatal diagnosis and the Prader-Willi syndrome.
Hum Genet. 1986 Mar;72(3):278 PMID: 3957352
Recurrence risk in de novo 21q21q translocation Down syndrome.
Am J Med Genet. 1985 Oct;22(2):417-8 PMID: 2931983
Recurrence risk in 21q/21q translocation of Down syndrome.
J Pediatr. 1982 Feb;100(2):243-5 PMID: 6460094

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00282561

Published

1986-11-00

Pages

327

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00282561 View journal details

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Approaches to the prenatal diagnosis of the Prader-Willi syndrome.

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