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Prader-Willi syndrome : and other chromosome 15q deletion disorders

The book presents the current knowledge on the Prader-Willi- and Angelman syndrome, two human chromosome disorders associated with mental retardation and other features. These two clinically dissimilar syndromes share unique genetics: in over half of the people with each of these disorders, the same deletion of the proximal long arm of chromosome 15 can be found. However, the deletion occurs in the paternally derived chromosome in Prader-Willi syndrome and in the maternally derived in Angelman syndrome. Emphasis is placed on the molecular genetics including genetic imprinting, recurrence risk determination, cytogenetics, and epidemiology of these disorders, as well as delineation of newly described clinical features.

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  • "Proceedings of the NATO Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders held at Noordwijkerhout (The Netherlands) from May 2-3, 1991"

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  • "The book presents the current knowledge on the Prader-Willi- and Angelman syndrome, two human chromosome disorders associated with mental retardation and other features. These two clinically dissimilar syndromes share unique genetics: in over half of the people with each of these disorders, the same deletion of the proximal long arm of chromosome 15 can be found. However, the deletion occurs in the paternally derived chromosome in Prader-Willi syndrome and in the maternally derived in Angelman syndrome. Emphasis is placed on the molecular genetics including genetic imprinting, recurrence risk determination, cytogenetics, and epidemiology of these disorders, as well as delineation of newly described clinical features."
  • "The book presents the current knowledge on the Prader-Willi- and Angelman syndrome, two human chromosome disorders associated with mental retardation and other features. These two clinically dissimilar syndromes share unique genetics: in over half of the people with each of these disorders, the same deletion of the proximal long arm of chromosome 15 can be found. However, the deletion occurs in the paternally derived chromosome in Prader-Willi syndrome and in the maternally derived in Angelman syndrome. Emphasis is placed on the molecular genetics including genetic imprinting, recurrence risk determination, cytogenetics, and epidemiology of these disorders, as well as delineation of newly described clinical features."@en

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  • "Kongress"
  • "Conference papers and proceedings"@en
  • "Conference papers and proceedings"
  • "Kongress (Noordwijkerhout, 1991)"
  • "Congresses"
  • "Electronic books"@en

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  • "Prader-Willi syndrome and other chromosome 15q deletion disorders : Proceedings of the NATO Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders held at Noordwijkerhout (The Netherlands) from May 2-3, 1991"
  • "Prader-Willi syndrome and other chromosome 15q deletion disorders : [proceedings of the NATO Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders held at Noordwijkerhout (The Netherlands) from May 2 - 3, 1991]"
  • "Prader-Willi syndrome and other chromosome 15q deletion disorders"
  • "Prader-Willi Syndrome and other chromosome 15q deletion disorders : [proceedings of the NATO Advanced Workshop on Prader-Willi Syndrome and other Chromosome 15q Disorders held at Noordwijkerhout (The Netherlands) from May 2 - 3, 1991]"
  • "Prader-Willi syndrome : and other chromosome 15q deletion disorders"@en
  • "Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders"

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