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D J Allingham-Hawkins

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Somatic Cell and Molecular Genetics|September 1, 1991
Somatic cell hybridization of Roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypesD J Allingham-Hawkins, D J Tomkins
American Journal of Human Genetics|July 1, 1995
FRAXE expansion is not a common etiological factor among developmentally delayed malesD J Allingham-Hawkins, P N Ray
American Journal of Medical Genetics|January 16, 1995
Heterogeneity in Roberts syndromeD J Allingham-Hawkins, D J Tomkins
American Journal of Medical Genetics|February 5, 1998
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometryD J Allingham-Hawkins, L K McGlynn-Steele, C A Brown, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.
Genetic Testing|January 6, 2001
Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndromeJ Tzountzouris, D Kennedy, M Skuterud, et al.
American Journal of Medical Genetics|April 20, 1999
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary dataD J Allingham-Hawkins, R Babul-Hirji, D Chitayat, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Somatic Cell and Molecular Genetics|September 1, 1991
Somatic cell hybridization of Roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypesD J Allingham-Hawkins, D J Tomkins
American Journal of Human Genetics|July 1, 1995
FRAXE expansion is not a common etiological factor among developmentally delayed malesD J Allingham-Hawkins, P N Ray
American Journal of Medical Genetics|January 16, 1995
Heterogeneity in Roberts syndromeD J Allingham-Hawkins, D J Tomkins
American Journal of Medical Genetics|February 5, 1998
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometryD J Allingham-Hawkins, L K McGlynn-Steele, C A Brown, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.
Genetic Testing|January 6, 2001
Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndromeJ Tzountzouris, D Kennedy, M Skuterud, et al.
American Journal of Medical Genetics|April 20, 1999
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary dataD J Allingham-Hawkins, R Babul-Hirji, D Chitayat, et al.
Pageof 1