L H Bowman|B Rabin|D Schlessinger - JoVE Visualize

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Human Molecular Genetics|September 25, 1997

Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.

Human Molecular Genetics|October 1, 1995

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3G B Ferrero, B Franco, E J Roth, et al.

The Journal of Clinical Endocrinology and Metabolism|October 13, 1998

Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.

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.

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Showing results (231-240 of 246) with videos related to

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Human Molecular Genetics|September 25, 1997

Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.

Human Molecular Genetics|October 1, 1995

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3G B Ferrero, B Franco, E J Roth, et al.

The Journal of Clinical Endocrinology and Metabolism|October 13, 1998

Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.

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.

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