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T Hassold

Showing results (41-50 of 58) with videos related to

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Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotypeN Krasikov, N Takaesu, T Hassold, et al.
Human Molecular Genetics|August 1, 1994
The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombinationM MacDonald, T Hassold, J Harvey, et al.
Human Genetics|October 1, 1994
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and livebornsM V Zaragoza, P A Jacobs, R S James, et al.
Human Genetics|January 28, 1999
FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidyM Hixon, E Millie, L A Judis, et al.
Journal of Medical Genetics|December 1, 1977
An interstitial deletion of chromosome 9 in a girl with multiple congenital anomaliesL Wisniewski, G Purdy, T Hassold, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocationsR S James, I K Temple, C Patch, et al.
Environmental and Molecular Mutagenesis|January 1, 1996
Aneuploidy in germ cells: etiologies and risk factorsJ B Bishop, V L Dellarco, T Hassold, et al.
Annals of Human Genetics|January 1, 1990
A centromere map of the X chromosome from trisomies of maternal originN E Morton, B J Keats, P A Jacobs, et al.
Progress in Clinical and Biological Research|January 1, 1989
Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long armM Buraczynska, G D Stewart, S Sherman, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotypeN Krasikov, N Takaesu, T Hassold, et al.
Human Molecular Genetics|August 1, 1994
The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombinationM MacDonald, T Hassold, J Harvey, et al.
Human Genetics|October 1, 1994
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and livebornsM V Zaragoza, P A Jacobs, R S James, et al.
Human Genetics|January 28, 1999
FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidyM Hixon, E Millie, L A Judis, et al.
Journal of Medical Genetics|December 1, 1977
An interstitial deletion of chromosome 9 in a girl with multiple congenital anomaliesL Wisniewski, G Purdy, T Hassold, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocationsR S James, I K Temple, C Patch, et al.
Environmental and Molecular Mutagenesis|January 1, 1996
Aneuploidy in germ cells: etiologies and risk factorsJ B Bishop, V L Dellarco, T Hassold, et al.
Annals of Human Genetics|January 1, 1990
A centromere map of the X chromosome from trisomies of maternal originN E Morton, B J Keats, P A Jacobs, et al.
Progress in Clinical and Biological Research|January 1, 1989
Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long armM Buraczynska, G D Stewart, S Sherman, et al.
Pageof 6