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15q12, 15q11-q13 GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia Prader-Willi syndrome *Gene map locus 15q12, 15q11-q13 Labhart-Willi syndrome PWS Prader-Labhart-Willi syndrome [Clinical features: diminished fetal activity; obesity; muscular hypotonia; mental retardation; short stature; hypogonadotropic hypogonadism; small hands and feet] [Inheritance: isolated cases] |
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Prader-Willi Syndrome |
Prader-Willi Syndrome |
Imprinting Mutations in Prader-Willi Syndrome |
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American Family Physician |
American Family Physician |
American Journal of Human Genetics |
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Prader-Willi syndrome |
Prader-Willi syndrome |
Prader-Willi syndrome |
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Neuroneonatology |
Neuroneonatology |
Neuroneonatology |
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16 images [ from 1 to 15 ] |
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