Prader-Willi syndrome and chromosome 15

Abstract

A chromosome 15 anomaly was observed in 12 of 20 patients, 17 of whom were clinically suspected of having Prader-Willi syndrome (PWS). The clinical features of eight cases with 15q11-12 deletion were very similar to those originally described in PWS. On the other hand, the group of normal karyotype patients is heterogeneous, and their features do not… (More)
DOI: 10.1007/BF00292367

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@article{Mattei2004PraderWilliSA, title={Prader-Willi syndrome and chromosome 15}, author={J. F. Mattei and M. G. Matt{\'e}i and Frederique Giraud}, journal={Human Genetics}, year={2004}, volume={64}, pages={356-362} }