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D H Ledbetter

Showing results (141-150 of 251) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequenceD T Pilz, M E Macha, K S Precht, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Organization of the HPRT gene and related sequences in the human genomeP I Patel, R L Nussbaum, P E gramson, et al.
Somatic Cell and Molecular Genetics|September 1, 1987
Assignment of human tryptophan hydroxylase locus to chromosome 11: gene duplication and translocation in evolution of aromatic amino acid hydroxylasesF D Ledley, H E Grenett, D P Bartos, et al.
American Journal of Medical Genetics|May 8, 1995
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter)A Scheuerle, J L Zenger-Hain, D L Van Dyke, et al.
The New England Journal of Medicine|February 5, 1981
Deletions of chromosome 15 as a cause of the Prader-Willi syndromeD H Ledbetter, V M Riccardi, S D Airhart, et al.
American Journal of Human Genetics|March 1, 1982
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 casesD H Ledbetter, J T Mascarello, V M Riccardi, et al.
Genomics|January 1, 1990
Complete cDNA sequence and chromosomal localization of mouse alpha 1-antitrypsinR N Sifers, F D Ledley, L Reed-Fourquet, et al.
Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Experimental Cell Research|April 1, 1987
Transformation of DNA repair-deficient human diploid fibroblasts with a simian virus 40 plasmidC M Wood, T L Timme, M M Hurt, et al.
Nature Genetics|September 1, 1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionJ S Sutcliffe, M Nakao, S Christian, et al.
Pageof 26

Showing results (141-150 of 251) with videos related to

Sort By:
Pageof 26
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequenceD T Pilz, M E Macha, K S Precht, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Organization of the HPRT gene and related sequences in the human genomeP I Patel, R L Nussbaum, P E gramson, et al.
Somatic Cell and Molecular Genetics|September 1, 1987
Assignment of human tryptophan hydroxylase locus to chromosome 11: gene duplication and translocation in evolution of aromatic amino acid hydroxylasesF D Ledley, H E Grenett, D P Bartos, et al.
American Journal of Medical Genetics|May 8, 1995
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter)A Scheuerle, J L Zenger-Hain, D L Van Dyke, et al.
The New England Journal of Medicine|February 5, 1981
Deletions of chromosome 15 as a cause of the Prader-Willi syndromeD H Ledbetter, V M Riccardi, S D Airhart, et al.
American Journal of Human Genetics|March 1, 1982
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 casesD H Ledbetter, J T Mascarello, V M Riccardi, et al.
Genomics|January 1, 1990
Complete cDNA sequence and chromosomal localization of mouse alpha 1-antitrypsinR N Sifers, F D Ledley, L Reed-Fourquet, et al.
Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Experimental Cell Research|April 1, 1987
Transformation of DNA repair-deficient human diploid fibroblasts with a simian virus 40 plasmidC M Wood, T L Timme, M M Hurt, et al.
Nature Genetics|September 1, 1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionJ S Sutcliffe, M Nakao, S Christian, et al.
Pageof 26