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M C Phelan

Showing results (11-20 of 44) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1989
Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXAS M Sauer, M C Phelan, C L Richer, et al.
Human Genetics|May 1, 1987
Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is presentC Schwartz, N Fitch, M C Phelan, et al.
American Journal of Medical Genetics|November 15, 1993
Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotypeR A Saul, R C Rogers, M C Phelan, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome and neoplasiaM C Phelan, R E Stevenson, J L Collins, et al.
American Journal of Medical Genetics|May 17, 1996
Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?A Brown, M C Phelan, S Patil, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of mosaicism for triploidy and trisomy 13M C Phelan, R Curtis Rogers, R C Michaelis, et al.
American Journal of Medical Genetics|September 15, 1993
Inverted duplication of 8p: ten new patients and review of the literatureG L Feldman, L Weiss, M C Phelan, et al.
American Journal of Obstetrics and Gynecology|August 3, 2001
Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous materialK L Jarrett, R C Michaelis, M C Phelan, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
American Journal of Medical Genetics|August 22, 1997
Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?R C Michaelis, S A Skinner, R Deason, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Cytogenetics and Cell Genetics|January 1, 1989
Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXAS M Sauer, M C Phelan, C L Richer, et al.
Human Genetics|May 1, 1987
Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is presentC Schwartz, N Fitch, M C Phelan, et al.
American Journal of Medical Genetics|November 15, 1993
Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotypeR A Saul, R C Rogers, M C Phelan, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome and neoplasiaM C Phelan, R E Stevenson, J L Collins, et al.
American Journal of Medical Genetics|May 17, 1996
Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?A Brown, M C Phelan, S Patil, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of mosaicism for triploidy and trisomy 13M C Phelan, R Curtis Rogers, R C Michaelis, et al.
American Journal of Medical Genetics|September 15, 1993
Inverted duplication of 8p: ten new patients and review of the literatureG L Feldman, L Weiss, M C Phelan, et al.
American Journal of Obstetrics and Gynecology|August 3, 2001
Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous materialK L Jarrett, R C Michaelis, M C Phelan, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
American Journal of Medical Genetics|August 22, 1997
Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?R C Michaelis, S A Skinner, R Deason, et al.
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