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Article

Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype.

American journal of medical genetics - 7 May 1999

Berends M J, Hordijk R, Scheffer H, Oosterwijk J C, Halley D J, Sorgedrager N

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Share to Abnormalities, Multiple
Share to Chromosomes, Human, Pair 14
Share to Genetic Markers
Share to Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Karyotyping

Share to Prader-Willi Syndrome

Share to Translocation, Genetic

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Identifiers

PMID: 10213052
DOI: 10.1002/(sici)1096-8628(19990507)84:1<76::aid-ajmg16>3.0.co;2-f

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype.PMID 10213052Read ↗

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