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American Journal of Medical Genetics
|
December 18, 1996
Familial ring (19) chromosome mosaicism: case report and review
W L Flejter, D Finlinson, S Root, et al.
American Journal of Medical Genetics
|
February 5, 1998
Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature review
W L Flejter, B Issa, B A Sullivan, et al.
Genes, Chromosomes & Cancer
|
November 1, 1992
Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13
W L Flejter, L D McDaniel, M Askari, et al.
American Journal of Medical Genetics
|
January 11, 1996
Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation
W L Flejter, P E Bennett-Baker, M Ghaziuddin, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Localization of the human HTF4 transcription factors 4 gene (TCF12) to chromosome 15q21
Y Zhang, W L Flejter, C L Barcroft, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24
W L Flejter, M Watkins, K J Abel, et al.
American Journal of Human Genetics
|
May 1, 1994
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications
J Leana-Cox, L Jenkins, C G Palmer, et al.
Prenatal Diagnosis
|
September 30, 2008
A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women
R Huang, T A Barber, M A Schmidt, et al.
Genomics
|
September 1, 1993
A radiation hybrid map of the BRCA1 region of chromosome 17q12-q21
K J Abel, M Boehnke, M Prahalad, et al.
Cancer
|
August 1, 1994
Familial breast cancer. Approaching the isolation of a susceptibility gene
B L Weber, K J Abel, L C Brody, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
December 18, 1996
Familial ring (19) chromosome mosaicism: case report and review
W L Flejter, D Finlinson, S Root, et al.
American Journal of Medical Genetics
|
February 5, 1998
Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature review
W L Flejter, B Issa, B A Sullivan, et al.
Genes, Chromosomes & Cancer
|
November 1, 1992
Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13
W L Flejter, L D McDaniel, M Askari, et al.
American Journal of Medical Genetics
|
January 11, 1996
Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation
W L Flejter, P E Bennett-Baker, M Ghaziuddin, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Localization of the human HTF4 transcription factors 4 gene (TCF12) to chromosome 15q21
Y Zhang, W L Flejter, C L Barcroft, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24
W L Flejter, M Watkins, K J Abel, et al.
American Journal of Human Genetics
|
May 1, 1994
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications
J Leana-Cox, L Jenkins, C G Palmer, et al.
Prenatal Diagnosis
|
September 30, 2008
A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women
R Huang, T A Barber, M A Schmidt, et al.
Genomics
|
September 1, 1993
A radiation hybrid map of the BRCA1 region of chromosome 17q12-q21
K J Abel, M Boehnke, M Prahalad, et al.
Cancer
|
August 1, 1994
Familial breast cancer. Approaching the isolation of a susceptibility gene
B L Weber, K J Abel, L C Brody, et al.
Page
of 3