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Christine J Shaw

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Human Molecular Genetics|February 7, 2004
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of diseaseChristine J Shaw, James R Lupski
Human Genetics|November 5, 2004
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanismsChristine J Shaw, James R Lupski
American Journal of Human Genetics|October 11, 2002
Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2Christine J Shaw, Weimin Bi, James R Lupski
American Journal of Human Genetics|May 19, 2004
Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substratesChristine J Shaw, Marjorie A Withers, James R Lupski
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2003
Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)]Lorraine Potocki, Christine J Shaw, Pawel Stankiewicz, et al.
Genome Research|November 3, 2004
Serial segmental duplications during primate evolution result in complex human genome architecturePawełl Stankiewicz, Christine J Shaw, Marjorie Withers, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
A girl with duplication 17p10-p12 associated with a dicentric chromosomeChristine J Shaw, Pawel Stankiewicz, John Christodoulou, et al.
American Journal of Human Genetics|November 26, 2003
Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2Weimin Bi, Sung-Sup Park, Christine J Shaw, et al.
Human Genetics|November 27, 2004
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Christine J Shaw, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|February 7, 2004
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of diseaseChristine J Shaw, James R Lupski
Human Genetics|November 5, 2004
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanismsChristine J Shaw, James R Lupski
American Journal of Human Genetics|October 11, 2002
Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2Christine J Shaw, Weimin Bi, James R Lupski
American Journal of Human Genetics|May 19, 2004
Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substratesChristine J Shaw, Marjorie A Withers, James R Lupski
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2003
Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)]Lorraine Potocki, Christine J Shaw, Pawel Stankiewicz, et al.
Genome Research|November 3, 2004
Serial segmental duplications during primate evolution result in complex human genome architecturePawełl Stankiewicz, Christine J Shaw, Marjorie Withers, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
A girl with duplication 17p10-p12 associated with a dicentric chromosomeChristine J Shaw, Pawel Stankiewicz, John Christodoulou, et al.
American Journal of Human Genetics|November 26, 2003
Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2Weimin Bi, Sung-Sup Park, Christine J Shaw, et al.
Human Genetics|November 27, 2004
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Christine J Shaw, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
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