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P L Pearson

Showing results (181-190 of 211) with videos related to

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American Journal of Human Genetics|March 1, 1985
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndromeU Francke, H D Ochs, B de Martinville, et al.
Cytogenetics and Cell Genetics|January 1, 1981
Characterization of the Philadelphia chromosome by gene mappingA H Geurts van Kessel, H ten Brinke, W A Boere, et al.
Thrombosis and Haemostasis|August 30, 1985
Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphismA H Bröcker-Vriends, E Briët, R Quadt, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13J H O van Tilburg, L A Sandkuijl, E Strengman, et al.
American Journal of Medical Genetics|July 1, 1993
Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21M J McGinniss, C Rosenberg, G Stetten, et al.
Nature Genetics|September 1, 1993
Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]B T Lamb, S S Sisodia, A M Lawler, et al.
Cell|November 21, 1986
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosomeG J van Ommen, J M Verkerk, M H Hofker, et al.
Nature|October 8, 1987
Germline mosaicism and Duchenne muscular dystrophy mutationsE Bakker, C Van Broeckhoven, E J Bonten, et al.
Genes, Brain, and Behavior|April 6, 2007
The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophreniaS C Bakker, M L C Hoogendoorn, J Hendriks, et al.
Genomics|April 1, 1993
Severe hemophilia A in a female by cryptic translocation: order and orientation of factor VIII within Xq28B R Migeon, M J McGinniss, S E Antonarakis, et al.
Pageof 22

Showing results (181-190 of 211) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|March 1, 1985
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndromeU Francke, H D Ochs, B de Martinville, et al.
Cytogenetics and Cell Genetics|January 1, 1981
Characterization of the Philadelphia chromosome by gene mappingA H Geurts van Kessel, H ten Brinke, W A Boere, et al.
Thrombosis and Haemostasis|August 30, 1985
Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphismA H Bröcker-Vriends, E Briët, R Quadt, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13J H O van Tilburg, L A Sandkuijl, E Strengman, et al.
American Journal of Medical Genetics|July 1, 1993
Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21M J McGinniss, C Rosenberg, G Stetten, et al.
Nature Genetics|September 1, 1993
Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]B T Lamb, S S Sisodia, A M Lawler, et al.
Cell|November 21, 1986
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosomeG J van Ommen, J M Verkerk, M H Hofker, et al.
Nature|October 8, 1987
Germline mosaicism and Duchenne muscular dystrophy mutationsE Bakker, C Van Broeckhoven, E J Bonten, et al.
Genes, Brain, and Behavior|April 6, 2007
The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophreniaS C Bakker, M L C Hoogendoorn, J Hendriks, et al.
Genomics|April 1, 1993
Severe hemophilia A in a female by cryptic translocation: order and orientation of factor VIII within Xq28B R Migeon, M J McGinniss, S E Antonarakis, et al.
Pageof 22