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Showing results (631-640 of 719) with videos related to

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Kidney International|April 29, 2011
L-carnitine is an osmotic agent suitable for peritoneal dialysisMario Bonomini, Assunta Pandolfi, Lorenzo Di Liberato, et al.
Journal of Human Genetics|August 3, 1999
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostosesK J Park, K H Shin, J L Ku, et al.
Gene|February 28, 2002
Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4BAlessandra Bolino, Valeria Marigo, Francesca Ferrera, et al.
European Journal of Human Genetics : EJHG|November 13, 2008
MET and autism susceptibility: family and case-control studiesInês Sousa, Taane G Clark, Claudio Toma, et al.
American Journal of Human Genetics|February 15, 2003
Use of multivariate linkage analysis for dissection of a complex cognitive traitAngela J Marlow, Simon E Fisher, Clyde Francks, et al.
Human Molecular Genetics|April 1, 1992
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombinationJ T Den Dunnen, P M Grootscholten, J G Dauwerse, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Xenotransplantation of canine, bovine, and porcine islets in diabetic rats without immunosuppressionR P Lanza, D H Butler, K M Borland, et al.
Cancer|May 15, 1993
Principles of psychosocial programming for children and cancerM A Chesler, S P Heiney, R Perrin, et al.
American Journal of Human Genetics|February 17, 2001
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeR Caraballo, S Pavek, A Lemainque, et al.
Genes, Brain, and Behavior|March 30, 2010
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3L Addis, A D Friederici, S A Kotz, et al.
Pageof 72

Showing results (631-640 of 719) with videos related to

Sort By:
Pageof 72
Kidney International|April 29, 2011
L-carnitine is an osmotic agent suitable for peritoneal dialysisMario Bonomini, Assunta Pandolfi, Lorenzo Di Liberato, et al.
Journal of Human Genetics|August 3, 1999
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostosesK J Park, K H Shin, J L Ku, et al.
Gene|February 28, 2002
Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4BAlessandra Bolino, Valeria Marigo, Francesca Ferrera, et al.
European Journal of Human Genetics : EJHG|November 13, 2008
MET and autism susceptibility: family and case-control studiesInês Sousa, Taane G Clark, Claudio Toma, et al.
American Journal of Human Genetics|February 15, 2003
Use of multivariate linkage analysis for dissection of a complex cognitive traitAngela J Marlow, Simon E Fisher, Clyde Francks, et al.
Human Molecular Genetics|April 1, 1992
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombinationJ T Den Dunnen, P M Grootscholten, J G Dauwerse, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Xenotransplantation of canine, bovine, and porcine islets in diabetic rats without immunosuppressionR P Lanza, D H Butler, K M Borland, et al.
Cancer|May 15, 1993
Principles of psychosocial programming for children and cancerM A Chesler, S P Heiney, R Perrin, et al.
American Journal of Human Genetics|February 17, 2001
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeR Caraballo, S Pavek, A Lemainque, et al.
Genes, Brain, and Behavior|March 30, 2010
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3L Addis, A D Friederici, S A Kotz, et al.
Pageof 72