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C Phelan

Showing results (121-130 of 164) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|August 26, 1999
Extraneural organ involvement in human rabiesA C Jackson, H Ye, C C Phelan, et al.
Epilepsia|October 7, 2019
Genetic attribution and perceived impact of epilepsy in multiplex epilepsy familiesDiana C Garofalo, Shawn T Sorge, Dale C Hesdorffer, 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.
Human Genetics|January 1, 1997
Exclusion of the phosphoinositide-specific phospholipase C beta 3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1G Weber, S Grimmond, J Lagercrantz, et al.
Journal of Internal Medicine|September 1, 1995
Candidate genes for multiple endocrine neoplasia type 1J Lagercrantz, C Larsson, S Grimmond, 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.
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.
Epilepsia|August 26, 2016
Depression and genetic causal attribution of epilepsy in multiplex epilepsy familiesShawn T Sorge, Dale C Hesdorffer, Jo C Phelan, et al.
Pageof 17

Showing results (121-130 of 164) with videos related to

Sort By:
Pageof 17
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 26, 1999
Extraneural organ involvement in human rabiesA C Jackson, H Ye, C C Phelan, et al.
Epilepsia|October 7, 2019
Genetic attribution and perceived impact of epilepsy in multiplex epilepsy familiesDiana C Garofalo, Shawn T Sorge, Dale C Hesdorffer, 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.
Human Genetics|January 1, 1997
Exclusion of the phosphoinositide-specific phospholipase C beta 3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1G Weber, S Grimmond, J Lagercrantz, et al.
Journal of Internal Medicine|September 1, 1995
Candidate genes for multiple endocrine neoplasia type 1J Lagercrantz, C Larsson, S Grimmond, 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.
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.
Epilepsia|August 26, 2016
Depression and genetic causal attribution of epilepsy in multiplex epilepsy familiesShawn T Sorge, Dale C Hesdorffer, Jo C Phelan, et al.
Pageof 17