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C Phelan

Showing results (131-140 of 164) with videos related to

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Genomics|April 10, 1995
Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C beta 3 gene (PLCB3)J Lagercrantz, E Carson, C Phelan, et al.
Journal of Medical Genetics|December 1, 1995
A large multisite cancer family is linked to BRCA2P Tonin, P Ghadirian, C Phelan, et al.
Language, Speech, and Hearing Services in Schools|April 23, 2026
Examining Relationships Between Caregiver Concerns and Family and Child Characteristics in Kindergarten Children at Risk for Language and Literacy DisordersMelissa C Phelan, Katharine M Radville, Julie A Wolter, et al.
Journal of Genetic Counseling|December 31, 2016
Research Participants' Preferences for Hypothetical Secondary Results from Genomic ResearchJulia Wynn, Josue Martinez, Jimmy Duong, et al.
Human Molecular Genetics|October 1, 1994
The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumoursG Weber, E Friedman, S Grimmond, 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.
Epilepsia|August 21, 2015
Genetic causal attribution of epilepsy and its implications for felt stigmaMaya Sabatello, Jo C Phelan, Dale C Hesdorffer, et al.
American Journal of Medical Genetics|July 15, 1994
Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, 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.
Oncogene|March 4, 1998
Identification of two distinct deleted regions on chromosome 13 in prostate cancerC Li, C Larsson, A Futreal, et al.
Pageof 17

Showing results (131-140 of 164) with videos related to

Sort By:
Pageof 17
Genomics|April 10, 1995
Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C beta 3 gene (PLCB3)J Lagercrantz, E Carson, C Phelan, et al.
Journal of Medical Genetics|December 1, 1995
A large multisite cancer family is linked to BRCA2P Tonin, P Ghadirian, C Phelan, et al.
Language, Speech, and Hearing Services in Schools|April 23, 2026
Examining Relationships Between Caregiver Concerns and Family and Child Characteristics in Kindergarten Children at Risk for Language and Literacy DisordersMelissa C Phelan, Katharine M Radville, Julie A Wolter, et al.
Journal of Genetic Counseling|December 31, 2016
Research Participants' Preferences for Hypothetical Secondary Results from Genomic ResearchJulia Wynn, Josue Martinez, Jimmy Duong, et al.
Human Molecular Genetics|October 1, 1994
The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumoursG Weber, E Friedman, S Grimmond, 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.
Epilepsia|August 21, 2015
Genetic causal attribution of epilepsy and its implications for felt stigmaMaya Sabatello, Jo C Phelan, Dale C Hesdorffer, et al.
American Journal of Medical Genetics|July 15, 1994
Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, 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.
Oncogene|March 4, 1998
Identification of two distinct deleted regions on chromosome 13 in prostate cancerC Li, C Larsson, A Futreal, et al.
Pageof 17