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H Ledbetter

Showing results (261-270 of 388) with videos related to

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Nature Genetics|August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethalityS Hirotsune, M W Fleck, M J Gambello, et al.
Neurology|August 3, 1999
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.
Journal of Medical Genetics|December 1, 1998
Two 22q telomere deletions serendipitously detected by FISHK S Precht, C M Lese, R P Spiro, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.
Oncogene Research|August 1, 1987
Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21D J Tweardy, L A Cannizzaro, A P Palumbo, et al.
Human Mutation|July 17, 2015
GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledgeBrianne E Kirkpatrick, Erin Rooney Riggs, Danielle R Azzariti, et al.
Neurology|July 27, 2001
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX geneL Demelas, G Serra, M Conti, et al.
Journal of Medical Genetics|March 19, 2002
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qJ A Fantes, S K Mewborn, C M Lese, et al.
Genomics|December 1, 1993
A somatic cell hybrid map of human chromosome 13S S Washington, A M Bowcock, S Gerken, et al.
American Journal of Human Genetics|December 1, 1991
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)T H Huang, J F Hejtmancik, A Edwards, et al.
Pageof 39

Showing results (261-270 of 388) with videos related to

Sort By:
Pageof 39
Nature Genetics|August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethalityS Hirotsune, M W Fleck, M J Gambello, et al.
Neurology|August 3, 1999
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.
Journal of Medical Genetics|December 1, 1998
Two 22q telomere deletions serendipitously detected by FISHK S Precht, C M Lese, R P Spiro, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.
Oncogene Research|August 1, 1987
Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21D J Tweardy, L A Cannizzaro, A P Palumbo, et al.
Human Mutation|July 17, 2015
GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledgeBrianne E Kirkpatrick, Erin Rooney Riggs, Danielle R Azzariti, et al.
Neurology|July 27, 2001
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX geneL Demelas, G Serra, M Conti, et al.
Journal of Medical Genetics|March 19, 2002
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qJ A Fantes, S K Mewborn, C M Lese, et al.
Genomics|December 1, 1993
A somatic cell hybrid map of human chromosome 13S S Washington, A M Bowcock, S Gerken, et al.
American Journal of Human Genetics|December 1, 1991
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)T H Huang, J F Hejtmancik, A Edwards, et al.
Pageof 39