B W Popovich - JoVE Visualize

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American Journal of Clinical Pathology|March 13, 2001

Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypesS B Parks, B W Popovich, R D Press

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2001

Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamicsR W Burman, K S Anoe, B W Popovich

American Journal of Human Genetics|December 1, 1986

Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene regionB W Popovich, D S Rosenblatt, A G Kendall, et al.

American Journal of Human Genetics|September 1, 1983

Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndromeB W Popovich, D S Rosenblatt, B A Cooper, et al.

Human Molecular Genetics|November 5, 1999

Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylationR W Burman, B W Popovich, P B Jacky, et al.

Gene|July 22, 1991

Problems encountered in detecting a targeted gene by the polymerase chain reactionH S Kim, B W Popovich, W R Shehee, et al.

American Journal of Human Genetics|May 1, 1995

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 geneF Quan, J Zonana, K Gunter, et al.

American Journal of Human Genetics|January 1, 1997

Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophyF Quan, J Janas, S Toth-Fejel, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 15, 1991

Correction of a human beta S-globin gene by gene targetingE G Shesely, H S Kim, W R Shehee, et al.

American Journal of Human Genetics|May 1, 1996

The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunctionS Toth-Fejel, S Olson, K Gunter, et al.

Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:

Pageof 2

American Journal of Clinical Pathology|March 13, 2001

Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypesS B Parks, B W Popovich, R D Press

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2001

Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamicsR W Burman, K S Anoe, B W Popovich

American Journal of Human Genetics|December 1, 1986

Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene regionB W Popovich, D S Rosenblatt, A G Kendall, et al.

American Journal of Human Genetics|September 1, 1983

Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndromeB W Popovich, D S Rosenblatt, B A Cooper, et al.

Human Molecular Genetics|November 5, 1999

Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylationR W Burman, B W Popovich, P B Jacky, et al.

Gene|July 22, 1991

Problems encountered in detecting a targeted gene by the polymerase chain reactionH S Kim, B W Popovich, W R Shehee, et al.

American Journal of Human Genetics|May 1, 1995

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 geneF Quan, J Zonana, K Gunter, et al.

American Journal of Human Genetics|January 1, 1997

Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophyF Quan, J Janas, S Toth-Fejel, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 15, 1991

Correction of a human beta S-globin gene by gene targetingE G Shesely, H S Kim, W R Shehee, et al.

American Journal of Human Genetics|May 1, 1996

The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunctionS Toth-Fejel, S Olson, K Gunter, et al.

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