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Showing results (251-260 of 368) with videos related to

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Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromesK Buiting, V Greger, B H Brownstein, et al.
International Journal of Cancer|April 13, 2005
Genomic gains on chromosome 1q in retinoblastoma: consequences on gene expression and association with clinical manifestationSandrine Gratias, Andreas Schüler, Ludger Klein Hitpass, et al.
International Journal of Cancer|April 26, 2005
Loss of heterozygosity of 1p in uveal melanomas with monosomy 3Thomas Häusler, Andreas Stang, Gerasimos Anastassiou, et al.
Plos Genetics|December 31, 2009
The human retinoblastoma gene is imprintedDeniz Kanber, Tea Berulava, Ole Ammerpohl, et al.
Cancer Research|July 15, 1994
Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridizationM R Speicher, G Prescher, S du Manoir, et al.
Human Molecular Genetics|May 1, 1995
The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instabilityA Klink, K Schiebel, M Winkelmann, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
Clinical utility gene card for: Prader-Willi SyndromeKarin Buiting, Suzanne B Cassidy, Daniel J Driscoll, et al.
Genomics|March 1, 1997
Genomic organization and promoter structure of the human EXT1 geneH J Lüdecke, J Ahn, X Lin, et al.
Pageof 37

Showing results (251-260 of 368) with videos related to

Sort By:
Pageof 37
Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromesK Buiting, V Greger, B H Brownstein, et al.
International Journal of Cancer|April 13, 2005
Genomic gains on chromosome 1q in retinoblastoma: consequences on gene expression and association with clinical manifestationSandrine Gratias, Andreas Schüler, Ludger Klein Hitpass, et al.
International Journal of Cancer|April 26, 2005
Loss of heterozygosity of 1p in uveal melanomas with monosomy 3Thomas Häusler, Andreas Stang, Gerasimos Anastassiou, et al.
Plos Genetics|December 31, 2009
The human retinoblastoma gene is imprintedDeniz Kanber, Tea Berulava, Ole Ammerpohl, et al.
Cancer Research|July 15, 1994
Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridizationM R Speicher, G Prescher, S du Manoir, et al.
Human Molecular Genetics|May 1, 1995
The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instabilityA Klink, K Schiebel, M Winkelmann, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
Clinical utility gene card for: Prader-Willi SyndromeKarin Buiting, Suzanne B Cassidy, Daniel J Driscoll, et al.
Genomics|March 1, 1997
Genomic organization and promoter structure of the human EXT1 geneH J Lüdecke, J Ahn, X Lin, et al.
Pageof 37