'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation.

Matsumura M, Kubota T, Hidaka E, Wakui K, Kadowaki S, Ueta I, Shimizu T, Ueno I, Yamauchi K, Herzing LB, Nurmi EL, Sutcliffe JS, Fukushima Y, Katsuyama T
Clin Genet. 2003 63 (1): 79-81

PMID: 12519378 · DOI:10.1034/j.1399-0004.2003.630114.x

MeSH Terms (11)

Chromosome Deletion Chromosomes, Human, Pair 15 Fetal Growth Retardation Genomic Imprinting Humans Infant Infant, Newborn In Situ Hybridization, Fluorescence Male Prader-Willi Syndrome Translocation, Genetic

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