A recurrent 15ql3.3 microdeletion syndrome associated with mental retardation and seizures

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Bibliographic Details
Published in:	Nature genetics Vol. 40; no. 3; pp. 322 - 328
Main Authors:	SHARP, Andrew J, MEFFORD, Heather C, BROOMER, Adam, CASUGA, Iris, YU WANG, CHUNLIN XIAO, BARBACIORU, Catalin, GIMELLI, Giorgio, DALLA BERNARDINA, Bernardo, TORNIERO, Claudia, GIORDA, Roberto, REGAN, Regina, LI, Kelly, MURDAY, Victoria, MANSOUR, Sahar, FICHERA, Marco, CASTIGLIA, Lucia, FAIFLA, Pinella, VENTURA, Mario, ZHAOSHI JIANG, COOPER, Gregory M, KNIGHT, Samantha J. L, ROMANO, Corrado, BAKER, Carl, ZUFFARDI, Orsetta, CAIFU CHEN, SCHWARTZ, Charles E, EICHLER, Evan E, SKINNER, Cindy, STEVENSON, Roger E, SCHROER, Richard J, NOVARA, Francesca, DE GREGORI, Manuela, CICCONE, Roberto
Format:	Journal Article
Language:	English
Published:	London Nature Publishing Group 2008
Subjects:	Adult and adolescent clinical studies Biological and medical sciences Complex syndromes Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Intellectual deficiency Medical genetics Medical sciences Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Nervous system diseases Convulsion Epilepsy Central nervous system disease Intellectual deficiency Developmental disorder Recurrent Neurological disorder Mental retardation Syndrome Cerebral disorder
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ISSN:	1061-4036 1546-1718