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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.

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.

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.

Molecular Psychiatry|September 30, 2003

Analysis of reelin as a candidate gene for autismE Bonora, K S Beyer, J A Lamb, et al.

Somatic Cell and Molecular Genetics|November 1, 1987

Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.

Genomics|July 24, 1998

Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome libraryP Y Woon, K Osoegawa, P J Kaisaki, et al.

Cancer Genetics and Cytogenetics|December 1, 1993

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2R F Suijkerbuijk, A M Meloni, R J Sinke, et al.

Human Molecular Genetics|July 1, 1994

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.

Pageof 29

Showing results (251-260 of 285) with videos related to

Sort By:

Pageof 29

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.

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.

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.

Molecular Psychiatry|September 30, 2003

Analysis of reelin as a candidate gene for autismE Bonora, K S Beyer, J A Lamb, et al.

Somatic Cell and Molecular Genetics|November 1, 1987

Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.

Genomics|July 24, 1998

Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome libraryP Y Woon, K Osoegawa, P J Kaisaki, et al.

Cancer Genetics and Cytogenetics|December 1, 1993

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2R F Suijkerbuijk, A M Meloni, R J Sinke, et al.

Human Molecular Genetics|July 1, 1994

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.

Pageof 29