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Prader-Willi syndrome and other chromosome 15q deletion disorders

Author: Suzanne B Cassidy; North Atlantic Treaty Organization. Scientific Affairs Division.
Publisher: Berlin ; New York : Springer-Verlag, ©1992.
Series: NATO ASI series., Series H,, Cell biology ;, vol. 61.
Edition/Format:   Print book : Conference publication : EnglishView all editions and formats
Summary:

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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Genre/Form: Conference papers and proceedings
Congresses
Material Type: Conference publication, Internet resource
Document Type: Book, Internet Resource
All Authors / Contributors: Suzanne B Cassidy; North Atlantic Treaty Organization. Scientific Affairs Division.
ISBN: 3540530959 9783540530954 0387530959 9780387530956
OCLC Number: 25282560
Notes: "Proceedings of the NATO Advanced Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders, held at Noordwijkerhout (the Netherlands), from May 2-3, 1991"--Title page verso.
"Published in cooperation with NATO Scientific Affairs Division."
Description: xii, 265 pages : illustrations ; 25 cm.
Contents: and Overview of Prader-Willi Syndrome.- Molecular Genetics of Prader-Willi and Angelman Syndromes.- Microdissection and Molecular Analysis of Proximal 15q.- The Irregular Inheritance of Angelman Syndrome and Prader-Willi Syndrome.- Characterization of cDNA Clones Corresponding to Genomic Loci Rearranged in Patients with Prader-Willi Syndrome.- Possible Genomic Imprinting at the Angelman Syndrome Gene Locus.- Molecular Analysis in Angelman Syndrome, Prader-Willi Syndrome and Potential Mouse Models.- Clinical, Molecular, and Cytogenetic Survey of Potential Prader-Willi Syndrome Patients.- Cytogenetics of Prader-Willi and Angelman Syndromes.- Cytogenetic Comparison between Prader-Willi and Angelman Syndromes.- Mosaicism for Deletion 15q11q13 in Sporadic and Familial Cases.- Prader-Willi Syndrome and Angelman Syndrome in Two Female Cousins as a Result of a Familial Translocation.- Implications for the Recurrence Risk in the Prader-Willi Syndrome on the Basis of Proposed Genomic Imprinting.- Clinical Aspects of Prader-Willi Syndrome: National Studies.- Diagnostic Criteria for Prader-Willi Syndrome.- An Australian Collaborative Study of Prader-Willi Syndrome Individuals and Their Families.- A Family Focused Care Model for Prader-Willi Syndrome in Norway: The Frambu Experience.- Prader-Willi Syndrome in Norway: An Epidemiological and Sociomedical Study.- A Multicenter Italian Study on Prader-Willi Syndrome.- A Comparison of Characteristics in 33 Japanese and 83 American Patients with Prader-Willi Syndrome.- Clinical Aspects of Prader-Willi Syndrome: Endocrine Studies.- Endocrine Physiology and Therapy in Prader-Willi Syndrome.- Growth Hormone Evaluation and Treatment in Prader-Willi Syndrome.- Diminished 24 Hour Urinary Growth Hormone Excretion in Patients with Prader-Willi Syndrome.- Clinical Aspects of Prader-Willi Syndrome: Physical Characteristics.- Energy Expenditure in the Prader-Willi Syndrome.- Antero-Posterior Cephalometric Analysis of the Craniofacial Complex in the Prader-Willi Syndrome.- Scoliosis and its Treatment in the Prader-Willi Syndrome.- Psychol0gical and Behavioral Aspects of Prader-Willi Syndrome.- Psychological Profile and Behavioral Characteristics in the Prader-Willi Syndrome.- The Use of Psychotropic Medications in Persons with Prader-Willi Syndrome.- Clinical Aspects of Angelman Syndrome.- Angelman Syndrome in the Adolescent and Young Adult.- Clinical Findings in Individuais with Angelman Syndrome without a Molecular Deletion or Uniparental Disomy.- Genetic Counseling for Angelman Syndrome When the Proband Has a Cytogenetic or Molecular Deletion.- Panel Discussion.- Current Understanding and Recurrence Risks of Prader-Willi and Angelman Syndromes.
Series Title: NATO ASI series., Series H,, Cell biology ;, vol. 61.
Responsibility: edited by Suzanne B. Cassidy.
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