Showing results (141-150 of 324) with videos related to
Sort By:
Pageof 33
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|June 5, 1998
Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2)A C Smith, E Dykens, F GreenbergAmerican Journal of Medical Genetics|April 1, 1988
Expanding the spectrum of the Perlman syndromeF Greenberg, K Copeland, M V GresikAmerican 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.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.Blood|January 1, 1988
Alteration and abnormal expression of the c-myc oncogene in human multiple myelomaP Selvanayagam, M Blick, F Narni, et al.Pageof 33