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D H Ledbetter

Showing results (41-50 of 251) with videos related to

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Human Genetics|June 1, 1996
Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalitiesY Ning, M Rosenberg, L G Biesecker, et al.
JAMA|December 15, 1993
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13W B Dobyns, O Reiner, R Carrozzo, et al.
Lancet (London, England)|December 6, 1997
Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndromeJ S Sutcliffe, M Han, S L Christian, et al.
American Journal of Human Genetics|April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1M E Goode, P vanTuinen, D H Ledbetter, et al.
American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.
Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.
Human Genetics|August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13A L Pettigrew, F Greenberg, C T Caskey, et al.
American Journal of Human Genetics|March 1, 1990
Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndromeD J Kwiatkowski, L Aklog, D H Ledbetter, et al.
Trends in Neurosciences|August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamicsR J Leventer, C Cardoso, D H Ledbetter, et al.
Genome Research|August 1, 1996
14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome regionS S Chong, A Tanigami, A V Roschke, et al.
Pageof 26

Showing results (41-50 of 251) with videos related to

Sort By:
Pageof 26
Human Genetics|June 1, 1996
Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalitiesY Ning, M Rosenberg, L G Biesecker, et al.
JAMA|December 15, 1993
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13W B Dobyns, O Reiner, R Carrozzo, et al.
Lancet (London, England)|December 6, 1997
Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndromeJ S Sutcliffe, M Han, S L Christian, et al.
American Journal of Human Genetics|April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1M E Goode, P vanTuinen, D H Ledbetter, et al.
American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.
Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.
Human Genetics|August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13A L Pettigrew, F Greenberg, C T Caskey, et al.
American Journal of Human Genetics|March 1, 1990
Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndromeD J Kwiatkowski, L Aklog, D H Ledbetter, et al.
Trends in Neurosciences|August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamicsR J Leventer, C Cardoso, D H Ledbetter, et al.
Genome Research|August 1, 1996
14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome regionS S Chong, A Tanigami, A V Roschke, et al.
Pageof 26