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C M Tuck-Muller

Showing results (21-30 of 33) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|May 1, 1994
An HLA-haplotype associated with preeclampsia and intrauterine growth retardationR D Peterson, C M Tuck-Muller, J A Spinnato, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
American Journal of Medical Genetics|March 1, 1994
Confirmation of proximal 1q duplication using fluorescence in situ hybridizationH Chen, C J Kusyk, C M Tuck-Muller, et al.
Molecular Biology & Medicine|December 1, 1990
Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13G Stetten, C M Tuck-Muller, K J Blakemore, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodiesE W Jabs, C M Tuck-Muller, G J Anhalt, et al.
Human Genetics|September 1, 1993
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridizationD A Batista, C M Tuck-Muller, J E Martinez, et al.
American Journal of Medical Genetics|February 13, 1995
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal glandH Chen, W H Hoffman, C J Kusyk, et al.
The New England Journal of Medicine|June 23, 1988
Partial monosomy 21, diminished activity of superoxide dismutase, and pulmonary oxygen toxicityA D Ackerman, J C Fackler, C M Tuck-Muller, et al.
Human Genetics|April 1, 1994
SRVX, a sex reversing locus in Xp21.2-->p22.11P Arn, H Chen, C M Tuck-Muller, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|May 1, 1994
An HLA-haplotype associated with preeclampsia and intrauterine growth retardationR D Peterson, C M Tuck-Muller, J A Spinnato, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
American Journal of Medical Genetics|March 1, 1994
Confirmation of proximal 1q duplication using fluorescence in situ hybridizationH Chen, C J Kusyk, C M Tuck-Muller, et al.
Molecular Biology & Medicine|December 1, 1990
Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13G Stetten, C M Tuck-Muller, K J Blakemore, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodiesE W Jabs, C M Tuck-Muller, G J Anhalt, et al.
Human Genetics|September 1, 1993
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridizationD A Batista, C M Tuck-Muller, J E Martinez, et al.
American Journal of Medical Genetics|February 13, 1995
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal glandH Chen, W H Hoffman, C J Kusyk, et al.
The New England Journal of Medicine|June 23, 1988
Partial monosomy 21, diminished activity of superoxide dismutase, and pulmonary oxygen toxicityA D Ackerman, J C Fackler, C M Tuck-Muller, et al.
Human Genetics|April 1, 1994
SRVX, a sex reversing locus in Xp21.2-->p22.11P Arn, H Chen, C M Tuck-Muller, et al.
Pageof 4