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Prader Willi Syndrome, see: Angelman syndrome
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Prader Willi SyndromePrader–Willi Syndrome (PWS) is a rare genetic disorder that is usually caused by chromosomal change, resulting in lifelong functional and cognitive impairments and life threatening obesity. PWS is fou [..]
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Prader Willi SyndromeAn autosomal dominant disorder caused by deletion of the proximal long arm of the paternal Chromosome 15 (15q11-q13) or by inheritance of both of the pair of Chromosomes 15 from the Mother (Uniparenta [..]
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