Prader-Willi and Angelman syndromes are two genetic diseases whose clinical diagnosis is often impaired by a wide variability in some clinical findings. New insights in the genetic basis of these disorders allow the proposition of a biological approach to detect almost all Prader-Willi syndrome patients and over 80% of Angelman syndrome patients. Moreover, the results of these tests are indispensable for the evaluation of the recurrence risk. (C) 1998, Elsevier, Paris.
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Univ Autonoma Barcelona, Fac Biociencies, Unitat Biol Cellular, Bellaterra, SpainUniv Autonoma Barcelona, Fac Biociencies, Unitat Biol Cellular, Bellaterra, Spain
Camprubi, Cristina
Coll, Maria Dolors
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Univ Autonoma Barcelona, Fac Biociencies, Unitat Biol Cellular, Bellaterra, SpainUniv Autonoma Barcelona, Fac Biociencies, Unitat Biol Cellular, Bellaterra, Spain
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Univ Calif San Francisco, Dept Pediat, Div Med Genet, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pediat, Div Med Genet, San Francisco, CA 94143 USA
Cassidy, Suzanne B.
Driscoll, Daniel J.
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Univ Florida, Coll Med, Dept Pediat, Div Genet & Metab, Gainesville, FL USAUniv Calif San Francisco, Dept Pediat, Div Med Genet, San Francisco, CA 94143 USA