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D Schlessinger

Showing results (251-260 of 263) with videos related to

Pageof 27
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Nature Genetics|August 1, 1996
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinJ Kere, A K Srivastava, O Montonen, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Physical map and cosmid contig encompassing a new interstitial deletion of the X-linked lymphoproliferative syndrome regionJ Lamartine, K E Nichols, L Yin, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
American Journal of Medical Genetics|December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated familiesR M Hughes-Benzie, G Pilia, J Y Xuan, et al.
Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsJ M Hoovers, L M Kalikin, L A Johnson, et al.
Genome Research|March 1, 1997
X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC contentR Nagaraja, S MacMillan, J Kere, et al.
Molecular Psychiatry|October 30, 2008
Genome-wide association scan for five major dimensions of personalityA Terracciano, S Sanna, M Uda, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Pageof 27

Showing results (251-260 of 263) with videos related to

Sort By:
Pageof 27
Nature Genetics|August 1, 1996
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinJ Kere, A K Srivastava, O Montonen, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Physical map and cosmid contig encompassing a new interstitial deletion of the X-linked lymphoproliferative syndrome regionJ Lamartine, K E Nichols, L Yin, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
American Journal of Medical Genetics|December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated familiesR M Hughes-Benzie, G Pilia, J Y Xuan, et al.
Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsJ M Hoovers, L M Kalikin, L A Johnson, et al.
Genome Research|March 1, 1997
X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC contentR Nagaraja, S MacMillan, J Kere, et al.
Molecular Psychiatry|October 30, 2008
Genome-wide association scan for five major dimensions of personalityA Terracciano, S Sanna, M Uda, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Pageof 27