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P A Jacobs

Showing results (71-80 of 175) with videos related to

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Human Genetics|September 12, 2000
Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotypeC Turner, N R Dennis, D H Skuse, et al.
American Journal of Medical Genetics|June 1, 1982
Marker X syndrome in an oriental family with probable transmission by a normal maleF A Rhoads, A C Oglesby, M Mayer, et al.
Human Genetics|January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndromeM Mayer, M A Abruzzo, P A Jacobs, et al.
Journal of Medical Genetics|February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingP A Jacobs, C Browne, N Gregson, et al.
Journal of Medical Genetics|March 1, 1971
Chromosome surveys in penal institutions and approved schoolsP A Jacobs, W H Price, S Richmond, et al.
Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.
Birth Defects Original Article Series|January 1, 1990
The parental origin of the missing or additional chromosome in 45,X and 47,XXX femalesT Hassold, K Arnovitz, P A Jacobs, et al.
Human Molecular Genetics|March 1, 1994
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutationJ N Macpherson, H Bullman, S A Youings, et al.
American Journal of Medical Genetics|April 1, 1992
Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotypeN R Dennis, G Curtis, J N Macpherson, et al.
Human Genetics|January 1, 1983
A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndromeP A Jacobs, M Mayer, J Matsuura, et al.
Pageof 18

Showing results (71-80 of 175) with videos related to

Sort By:
Pageof 18
Human Genetics|September 12, 2000
Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotypeC Turner, N R Dennis, D H Skuse, et al.
American Journal of Medical Genetics|June 1, 1982
Marker X syndrome in an oriental family with probable transmission by a normal maleF A Rhoads, A C Oglesby, M Mayer, et al.
Human Genetics|January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndromeM Mayer, M A Abruzzo, P A Jacobs, et al.
Journal of Medical Genetics|February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingP A Jacobs, C Browne, N Gregson, et al.
Journal of Medical Genetics|March 1, 1971
Chromosome surveys in penal institutions and approved schoolsP A Jacobs, W H Price, S Richmond, et al.
Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.
Birth Defects Original Article Series|January 1, 1990
The parental origin of the missing or additional chromosome in 45,X and 47,XXX femalesT Hassold, K Arnovitz, P A Jacobs, et al.
Human Molecular Genetics|March 1, 1994
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutationJ N Macpherson, H Bullman, S A Youings, et al.
American Journal of Medical Genetics|April 1, 1992
Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotypeN R Dennis, G Curtis, J N Macpherson, et al.
Human Genetics|January 1, 1983
A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndromeP A Jacobs, M Mayer, J Matsuura, et al.
Pageof 18