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M C Phelan

Showing results (21-30 of 44) with videos related to

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Pediatric Research|February 1, 1997
A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiencyS M Willi, Y Zhang, J B Hill, et al.
Clinical Genetics|February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1J C Marinoni, R E Stevenson, J P Evans, et al.
Human Genetics|September 1, 1988
The parental origin and mechanism of formation of three dicentric X chromosomesM C Phelan, L A Prouty, R E Stevenson, et al.
American Journal of Medical Genetics|January 2, 1995
Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion regionR C Michaelis, S A Skinner, B A Lethco, et al.
Prenatal Diagnosis|December 17, 1998
FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16M C Phelan, W Blackburn, R C Rogers, et al.
American Journal of Medical Genetics|July 15, 1992
Cytogenetic, biochemical, and molecular analyses of a 22q13 deletionM C Phelan, G R Thomas, R A Saul, et al.
Pediatrics|September 1, 1986
Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissuesR E Stevenson, K L Jones, M C Phelan, et al.
Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: linkage analysis in black and white populationsC E Schwartz, M C Phelan, C Brightharp, et al.
American Journal of Human Genetics|October 1, 1993
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndromeA McConkie-Rosell, A M Lachiewicz, G A Spiridigliozzi, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Pediatric Research|February 1, 1997
A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiencyS M Willi, Y Zhang, J B Hill, et al.
Clinical Genetics|February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1J C Marinoni, R E Stevenson, J P Evans, et al.
Human Genetics|September 1, 1988
The parental origin and mechanism of formation of three dicentric X chromosomesM C Phelan, L A Prouty, R E Stevenson, et al.
American Journal of Medical Genetics|January 2, 1995
Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion regionR C Michaelis, S A Skinner, B A Lethco, et al.
Prenatal Diagnosis|December 17, 1998
FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16M C Phelan, W Blackburn, R C Rogers, et al.
American Journal of Medical Genetics|July 15, 1992
Cytogenetic, biochemical, and molecular analyses of a 22q13 deletionM C Phelan, G R Thomas, R A Saul, et al.
Pediatrics|September 1, 1986
Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissuesR E Stevenson, K L Jones, M C Phelan, et al.
Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: linkage analysis in black and white populationsC E Schwartz, M C Phelan, C Brightharp, et al.
American Journal of Human Genetics|October 1, 1993
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndromeA McConkie-Rosell, A M Lachiewicz, G A Spiridigliozzi, et al.
Pageof 5