Paper Details

Paper Title

Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome.

Paper Journal Title

European Journal of Human Genetics

Paper Citation Count

Paper Publication Year

2005

Bio Mention

-, DHPLC, PWS, Prader-Willi syndrome, SNRPN, SNRPN alleles, SNURF, blood cells, chromosomes 15, patient, peripheral blood DNA, woman

Mesh Descriptor

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