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P A Jacobs

Showing results (151-160 of 175) with videos related to

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Annals of Human Genetics|April 22, 2006
An investigation of FRAXA intermediate allele phenotype in a longitudinal sampleS Ennis, A Murray, S Youings, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
The New England Journal of Medicine|March 29, 1979
More on marker X chromosomes, mental retardation and macro-orchidismP A Jacobs, M Mayer, E Rudak, et al.
Annals of Human Genetics|May 1, 1975
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2M A Mace, J Noades, E B Robson, et al.
Annals of Human Genetics|October 1, 1980
A cytogenetic study of 1000 spontaneous abortionsT Hassold, N Chen, J Funkhouser, et al.
American Journal of Human Genetics|July 10, 2001
Maternal folate polymorphisms and the etiology of human nondisjunctionT J Hassold, L C Burrage, E R Chan, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Nondisjunction of chromosome 21N Takaesu, P A Jacobs, A Cockwell, et al.
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.
Pageof 18

Showing results (151-160 of 175) with videos related to

Sort By:
Pageof 18
Annals of Human Genetics|April 22, 2006
An investigation of FRAXA intermediate allele phenotype in a longitudinal sampleS Ennis, A Murray, S Youings, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
The New England Journal of Medicine|March 29, 1979
More on marker X chromosomes, mental retardation and macro-orchidismP A Jacobs, M Mayer, E Rudak, et al.
Annals of Human Genetics|May 1, 1975
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2M A Mace, J Noades, E B Robson, et al.
Annals of Human Genetics|October 1, 1980
A cytogenetic study of 1000 spontaneous abortionsT Hassold, N Chen, J Funkhouser, et al.
American Journal of Human Genetics|July 10, 2001
Maternal folate polymorphisms and the etiology of human nondisjunctionT J Hassold, L C Burrage, E R Chan, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Nondisjunction of chromosome 21N Takaesu, P A Jacobs, A Cockwell, et al.
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.
Pageof 18