The Year in Human and Medical Genetics 2009
January 2009, Wiley-Blackwell
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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.