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Showing results (121-130 of 136) with videos related to

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Journal of Medical Genetics|March 1, 1995
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndromeJ N Macpherson, G Curtis, J A Crolla, et al.
Human Genetics|July 8, 1998
A study of females with deletions of the short arm of the X chromosomeR S James, B Coppin, P Dalton, et al.
American Journal of Human Genetics|September 1, 1991
Trisomy 21: association between reduced recombination and nondisjunctionS L Sherman, N Takaesu, S B Freeman, et al.
Chemical Communications (Cambridge, England)|January 29, 2010
Molecular sieve properties of mesoporous silica with intraporous nanocarbonF de Clippel, A Harkiolakis, X Ke, et al.
American Journal of Human Genetics|April 1, 1995
Cytogenetic and molecular studies of Down syndrome individuals with leukemiaJ J Shen, B J Williams, A Zipursky, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markersI Oberlé, R Heilig, J P Moisan, et al.
Cell|February 22, 1991
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndromeM V Bell, M C Hirst, Y Nakahori, et al.
Nature|June 12, 1997
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive functionD H Skuse, R S James, D V Bishop, et al.
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.
Pageof 14

Showing results (121-130 of 136) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|March 1, 1995
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndromeJ N Macpherson, G Curtis, J A Crolla, et al.
Human Genetics|July 8, 1998
A study of females with deletions of the short arm of the X chromosomeR S James, B Coppin, P Dalton, et al.
American Journal of Human Genetics|September 1, 1991
Trisomy 21: association between reduced recombination and nondisjunctionS L Sherman, N Takaesu, S B Freeman, et al.
Chemical Communications (Cambridge, England)|January 29, 2010
Molecular sieve properties of mesoporous silica with intraporous nanocarbonF de Clippel, A Harkiolakis, X Ke, et al.
American Journal of Human Genetics|April 1, 1995
Cytogenetic and molecular studies of Down syndrome individuals with leukemiaJ J Shen, B J Williams, A Zipursky, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markersI Oberlé, R Heilig, J P Moisan, et al.
Cell|February 22, 1991
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndromeM V Bell, M C Hirst, Y Nakahori, et al.
Nature|June 12, 1997
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive functionD H Skuse, R S James, D V Bishop, et al.
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.
Pageof 14