Year in Human and Medical Genetics 2009

Häftad, Engelska, 2009

Del i serien Annals of the New York Academy of Sciences

1 138 kr

Tillfälligt slut

Beskrivning

This is the inaugural volume for a new annual review serving the medical genetics community. This annual volume will feature in-depth scholarly reviews of the most timely and important topics and issues affecting this field. Special Offer from the New York Academy of Sciences: Order this volume at a discount and become a NYAS Individual Member free. Click here to find out more on the NYAS site. Follow the instructions for adding individual membership to your shopping cart and choose this volume, which will show as being free. Offer not applicable in conjunction with a Student & Postdoc Membership.NOTE: Annals volumes are available for sale as individual books or as a journal. For information on institutional journal subscriptions, please visit www.blackwellpublishing.com/nyas.ACADEMY MEMBERS: Please contact the New York Academy of Sciences directly to place your order (www.nyas.org). Members of the New York Academy of Science receive full-text access to the Annals online and discounts on print volumes. Please visit http://www.nyas.org/MemberCenter/Join.aspx for more information about becoming a member.

Produktinformation

Utgivningsdatum:2009-02-20
Mått:179 x 255 x 8 mm
Vikt:381 g
Format:Häftad
Språk:Engelska
Serie:Annals of the New York Academy of Sciences
Antal sidor:352
Förlag:John Wiley and Sons Ltd
ISBN:9781573317313

Utforska kategorier

Biologi inom Naturvetenskap och teknik

Mer om författaren

Moyra Smith- Irvine, CA - is a professor of pediatrics and human genetics at the University of California, Irvine, School of Medicine.

Innehållsförteckning

Preface: Moyra Smith. 1. Highlights in Human Genetics in 2007–2008: Moyra Smith.2. On the Molecular Etiology of Cornelia de Lange Syndrome: Dale Dorsett and Ian D. Krantz.3. Progress in the Understanding of the Genetic Etiology of Vertebral Segmentation Disorders in Humans: Philip F. Giampietro, Sally L. Dunwoodie, Kenro Kusumi, Olivier Pourquié, Olivier Tassy, Amaka C. Offiah, Alberto S. Cornier, Benjamin A. Alman, Robert D. Blank, Cathleen L. Raggio, Ingrid Glurich, and Peter D. Turnpenny.4. Chimerism in Black Southern African Patients with True Hermaphroditism: 46,XX/47XY,+21 and 46,XX/46,XY: M. Ramsay, W. Pfaffenzeller, E. Kotze, L. Bhengu, F. Essop, and T. de Ravel.5. Combined Tarsal and Carpal Tunnel Syndrome in Mucolipidosis Type III: A Case Study and Review: Izelle Smuts, Denise Potgieter, and Francois Hendrikus van der Westhuizen.6. Clinical Characteristics of an Afrikaner Founder Population Schizophrenia Genetic Sample: Johannes Lodewikus Roos, Herman Walter Pretorius, and Maria Karayiorgou.7. Nuclear and Mitochondrial Genome Defects in Autisms: Moyra Smith, M. Anne Spence, and Pamela Flodman.8. Genetic Calcium Signaling Abnormalities in the CNS: Seizures, Migraine, and Autism: J. Jay Gargus.9. Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies: Lisa Edelmann and Kurt Hirschhorn.Index of Contributors.