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2009 OCT 26 ... contact J.G. Gleeson, University of California, Howard Hughes Med Institute, Neurogenetics Laboratory, Dept. of Neuroscience & Pediatrics, La Jolla, CA 92093, USA. ...
2009 OCT 20 ... Pediatric Neurology at Texas Children's Hospital, The Blue Bird Circle Developmental Neurogenetics Laboratory at Baylor College of Medicine, and The Blue Bird Circle Rett Center. In the ...
2009 OCT 27 ... of their research in Genetics (A Drosophila Resource of Transgenic RNAi Lines for Neurogenetics. Genetics, 2009;182(4):1089-1100). For additional information, contact N. ...
2009 NOV 16 ... For additional information, contact J.G. Gleeson, University of California, Neurogenetics Laboratory, Howard Hughes Med Institute, Dept. of Pediatrics & Neuroscience, Leichtag ...
2009 OCT 20 ... identical MAPT mutations." Colombo and colleagues published their study in neurogenetics (Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal ...
2009 NOV 16 ... Disease, Enzymes, Epilepsy, Genetics, Machado-Joseph Disease, Mitochondrial Disease, Neurogenetics, Neurology, Polymerase. This article was prepared by Pain & Central Nervous ...
2009 NOV 9 ... For additional information, contact D.K. Lahiri, Laboratory of Molecular Neurogenetics, Dept. of Psychiatry, Institute of Psychiatric Research, Indiana University School of ...
2009 OCT 19 ... to nearby regions in Spain." Mata and colleagues published their study in neurogenetics (Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the ...
2009 NOV 16 ... For more information, contact E. Sidransky, NHGRI, Sect Molecular Neurogenetics, Medical Genetics Branch, Rm 1A213, 35 Convent Dr., Bethesda, MD 20892, USA. ...
2009 OCT 20 ... information, contact S.M. Oshea, Max Planck Institute Biophysics, Dept. of Molecular Neurogenetics, Max von Laue Str 3, D-60438 Frankfurt, Germany. Publisher contact ...
2009 OCT 20 ... of FGF14 can cause SCA27." Misceo and colleagues published their study in neurogenetics (SCA27 caused by a chromosome translocation: further delineation of the phenotype....
2009 NOV 16 ... For additional information, contact L. Ma, University of California, Zilkha Neurogenetics Institute, Keck School Medical, Graduate Program Neuroscience, Dept. of Cell & ...
2009 OCT 19 ... caused by MFSD8 mutations: a common theme emerging,' is newly published data in neurogenetics. "Neuronal ceroid lipofuscinoses (NCLs) are a group of lysosomal neurodegenerative ...
2009 OCT 19 ... syndrome." Wang and colleagues published the results of their research in neurogenetics (Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and ...
2009 OCT 19 ... of both." de and colleagues published the results of their research in neurogenetics (Movement disorder and neuronal migration disorder due to ARFGEF2 mutation....
2009 OCT 20 ... to the phenotype." Brusse and colleagues published their study in neurogenetics (A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic ...
2009 OCT 19 ... West African population." Traore and colleagues published their study in neurogenetics (Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora ...
2009 OCT 19 ... are discussed in a new report. According to recent research published in the journal neurogenetics, "Snyder-Robinson syndrome (SRS) is a form of X-linked mental retardation resulting ...
