A case of Prader Willi syndrome with del 15 (q11-->q13).

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A case of Prader Willi syndrome with del 15 (q11-->q13).
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Cytogenetic analysis was performed on a four-year-old girl with obesity, mental retardation, recurrent febrile convulsions and a provisional diagnosis of Prader Willi syndrome. High-resolution banding was done to observe the subchromosomal deletion. An interstitial deletion (q11-->q13) on one of the 15th chromosomes was observed in all metaphases.
Tunçman G, Tükün A, Yalaz K, and Bökesoy I
The Turkish journal of pediatrics 35(4):333-6, 1993 - Who cited this? | PubMed ID: 8160287 | Fulltext
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