Prader-Willi Syndrome: And Other Chromosome 15q Deletion Disorders

Author:   Suzanne B. Cassidy
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Volume:   61
ISBN:  

9783540530954


Pages:   277
Publication Date:   13 April 1992
Format:   Hardback
Availability:   Out of stock   Availability explained
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

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Prader-Willi Syndrome: And Other Chromosome 15q Deletion Disorders


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Author:   Suzanne B. Cassidy
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Imprint:   Springer-Verlag Berlin and Heidelberg GmbH & Co. K
Volume:   61
Weight:   0.590kg
ISBN:  

9783540530954


ISBN 10:   3540530959
Pages:   277
Publication Date:   13 April 1992
Audience:   College/higher education ,  Professional and scholarly ,  Postgraduate, Research & Scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Out of stock   Availability explained
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

Table of 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.

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