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Human Genetics|August 4, 2005
Haplotypes within genes of beta-chemokines in 17q11 are associated with multiple sclerosis: a second phase studyTamara Vyshkina, Bernadette KalmanHuman Genetics|August 4, 2005
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomasTeresita Díaz de Ståhl, Caisa M Hansson, Cecilia de Bustos, et al.Human Genetics|August 4, 2005
Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorderTomoko Makishima, Clara I Rodriguez, Nahid G Robertson, et al.Human Genetics|September 27, 2005
Genetic variability in a genomic region with long-range linkage disequilibrium reveals traces of a bottleneck in the history of the European populationClaudia Schmegner, Josef Hoegel, Walther Vogel, et al.Human Genetics|June 1, 1992
Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in QuebecL R Simard, F Gingras, N Delvoye, et al.Human Genetics|June 1, 1992
Familial pericentric inversion (3)(p12q24)L Lindberg, K Pelto, G H BorgströmHuman Genetics|March 19, 2005
Extensively high load of internal tumors determined by whole body MRI scanning in a patient with neurofibromatosis type 1 and a non-LCR-mediated 2-Mb deletion in 17q11.2Hildegard Kehrer-Sawatzki, Lan Kluwe, Carsten Fünsterer, et al.Human Genetics|April 14, 2005
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson diseaseMaher A Noureddine, Xue-Jun Qin, Sofia A Oliveira, et al.Human Genetics|February 16, 2005
Molecular distinction between true centric fission and pericentric duplication-fissionJo Perry, Sara Nouri, Phung La, et al.Human Genetics|April 17, 1979
Phosphofructokinase (PFK) isozymes in man. I. Studies of adult human tissuesA Kahn, M C Meienhofer, D Cottreau, et al.Pageof 957