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Human Molecular Genetics|February 1, 1997
The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmissionA Murray, J N Macpherson, M C Pound, et al.Genes, Chromosomes & Cancer|April 1, 1992
Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemiaB J Lorber, S B Freeman, T Hassold, et al.European Journal of Human Genetics : EJHG|August 22, 2000
Stability and haplotype analysis of the FRAXE regionA Murray, S Ennis, S A Youings, et al.Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypesB R Migeon, S Luo, B A Stasiowski, et al.Human Genetics|January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting malesS L Sherman, P A Jacobs, N E Morton, et al.Proceedings of the National Academy of Sciences of the United States of America|January 22, 1998
FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disabilityJ W Teague, N E Morton, N R Dennis, et al.Journal of Medical Genetics|January 7, 2005
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesS M Gribble, E Prigmore, D C Burford, et al.Genetics|May 1, 1972
Segmental aneuploidy and the genetic gross structure of the Drosophila genomeD L Lindsley, L Sandler, B S Baker, et al.Pageof 17