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The Year in Human and Medical Genetics 2009, Volume 1151

Moyra Smith (Editor)
ISBN: 978-1-57331-731-3
352 pages
January 2009, Wiley-Blackwell
The Year in Human and Medical Genetics 2009, Volume 1151 (1573317314) cover image


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.

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Table of Contents

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.

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The Year in Human and Medical Genetics 2009, Volume 1151 (US $149.95)

-and- The Year in Cognitive Neuroscience 2012, Volume 1251 (US $145.00)

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