1. A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband. (12th September 2011) Authors: Wilson, Nicole K. A.; Lee, Yohan; Long, Robert; Hermetz, Karen; Rudd, M. Katharine; Miller, Rachel; Rapoport, Judith L.; Addington, Anjené M. Other Names: Cheng C.-W. Academic Editor.; Ergul E. Academic Editor.; Steinberger D. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosome Deletion of 14q32.33 Detected by Array Comparative Genomic Hybridization in a Patient with Features of Dubowitz Syndrome. (28th September 2011) Authors: Darcy, Diana C.; Rosenthal, Scott; Wallerstein, Robert J. Other Names: Blakemore A. Academic Editor.; de Nanclares G. Academic Editor.; Huang C.-S. Academic Editor.; Rajcan-Separovic E. Academic Editor.; Sazci A. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical Expression of an Inherited Unbalanced Translocation in Chromosome 6. (25th September 2011) Authors: Ganguly, Bani Bandana; Kadam, Vijay; Kadam, Nitin N. Other Names: López Ginés C. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Inheritance of a Ring Chromosome 21 in a Couple Undergoing In Vitro Fertilization (IVF): A Case Report. (31st July 2011) Authors: Mazzaschi, Roberto L. P.; Love, Donald R.; Hayes, Ian; George, Alice Other Names: Cotter P. D. Academic Editor.; Mittal B. Academic Editor.; Sazci A. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Intrafamilial Variability of Early-Onset Diabetes due to an INS Mutation. (12th June 2011) Authors: Fredheim, Siri; Svensson, Jannet; Pørksen, Sven; Hansen, Lars; Hansen, Torben; Pedersen, Oluf Borbye; Mortensen, Henrik Bindesbøl; Barbetti, Fabrizio; Nielsen, Lotte Brøndum Other Names: Chae S.-C. Academic Editor.; Ishiguro H. Academic Editor.; Shotelersuk V. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Synchronous Pulmonary Squamous Cell Carcinoma and Mantle Cell Lymphoma of the Lymph Node. (2nd July 2011) Authors: Sun, Yu; Shi, Yun-Fei; Zhou, Li-Xin; Chen, Ke-Neng; Li, Xiang-Hong Other Names: Ergul E. Academic Editor.; Saccucci P. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Vici Syndrome: A Rare Autosomal Recessive Syndrome with Brain Anomalies, Cardiomyopathy, and Severe Intellectual Disability. (31st May 2011) Authors: Rogers, R. Curtis; Aufmuth, Bridgette; Monesson, Stephanie Other Names: Baumer A. Academic Editor.; Bunyan D. J. Academic Editor.; Mittal B. Academic Editor.; Sazci A. Academic Editor. Journal: Case reports in genetics Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗