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Human Genetics|January 1, 1983
Expression of the fragile (X) chromosome in an interspecific somatic cell hybridR L Nussbaum, S D Airhart, D H LedbetterHuman 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.American Journal of Medical Genetics|September 1, 1988
The impact of MSAFP screening on genetic services, 1984-1986F GreenbergAmerican Journal of Medical Genetics|December 1, 1987
Choanal atresia and athelia: methimazole teratogenicity or a new syndrome?F GreenbergAmerican 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.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.Pageof 33