A R Brothman|D L Persons|L G Shaffer - JoVE Visualize

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Human Molecular Genetics|February 5, 1999

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletionsY Q Wu, H A Heilstedt, J A Bedell, et al.

Blood|November 24, 2001

Benefit of cyclosporine modulation of drug resistance in patients with poor-risk acute myeloid leukemia: a Southwest Oncology Group studyA F List, K J Kopecky, C L Willman, et al.

Human Mutation|June 20, 2003

Epigenetic detection of human chromosome 14 uniparental disomyS K Murphy, A A Wylie, K J Coveler, et al.

Human Molecular Genetics|December 23, 1999

Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphaseE Earle, A Saxena, A MacDonald, et al.

Clinical Genetics|March 21, 2002

Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotypeP Stankiewicz, S S Parka, S E Holder, et al.

American Journal of Human Genetics|December 1, 1999

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocationL Edelmann, E Spiteri, N McCain, et al.

American Journal of Human Genetics|August 1, 1997

A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.

Annals of Neurology|May 13, 1999

Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestationsK Inoue, H Osaka, K Imaizumi, et al.

Archives of Pathology & Laboratory Medicine|May 11, 1999

Extensive analysis of mosaicism in a case of Turner syndrome: the experience of 287 cytogenetic laboratories. College of American Pathologists/American College of Medical Genetics Cytogenetics Resource CommitteeJ P Park, A R Brothman, M G Butler, et al.

American Journal of Human Genetics|January 1, 1995

The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2K S Chen, P H Gunaratne, J D Hoheisel, et al.

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Showing results (191-200 of 215) with videos related to

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Pageof 22

Human Molecular Genetics|February 5, 1999

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletionsY Q Wu, H A Heilstedt, J A Bedell, et al.

Blood|November 24, 2001

Benefit of cyclosporine modulation of drug resistance in patients with poor-risk acute myeloid leukemia: a Southwest Oncology Group studyA F List, K J Kopecky, C L Willman, et al.

Human Mutation|June 20, 2003

Epigenetic detection of human chromosome 14 uniparental disomyS K Murphy, A A Wylie, K J Coveler, et al.

Human Molecular Genetics|December 23, 1999

Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphaseE Earle, A Saxena, A MacDonald, et al.

Clinical Genetics|March 21, 2002

Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotypeP Stankiewicz, S S Parka, S E Holder, et al.

American Journal of Human Genetics|December 1, 1999

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocationL Edelmann, E Spiteri, N McCain, et al.

American Journal of Human Genetics|August 1, 1997

A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.

Annals of Neurology|May 13, 1999

Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestationsK Inoue, H Osaka, K Imaizumi, et al.

Archives of Pathology & Laboratory Medicine|May 11, 1999

Extensive analysis of mosaicism in a case of Turner syndrome: the experience of 287 cytogenetic laboratories. College of American Pathologists/American College of Medical Genetics Cytogenetics Resource CommitteeJ P Park, A R Brothman, M G Butler, et al.

American Journal of Human Genetics|January 1, 1995

The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2K S Chen, P H Gunaratne, J D Hoheisel, et al.

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