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C Shuman

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

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
Genomics|June 21, 2001
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutationsM Li, J Squire, C Shuman, et al.
Gynecologic Oncology|March 4, 2017
Corrigendum to "The sooner the better: Genetic testing following ovarian cancer diagnosis" [Gynecol. Oncol. 137 (2015) 423-429]E Fox, J McCuaig, R Demsky, et al.
European Journal of Medical Genetics|December 4, 2018
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatricsM J Szego, M S Meyn, C Shuman, et al.
Gynecologic Oncology|April 15, 2015
The sooner the better: Genetic testing following ovarian cancer diagnosisE Fox, J McCuaig, R Demsky, et al.
Clinical Genetics|July 22, 2014
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelinesJ A Anderson, R Z Hayeems, C Shuman, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Journal of Medical Ethics|November 27, 2016
Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?J A Anderson, M S Meyn, C Shuman, et al.
American Journal of Medical Genetics|July 31, 2001
GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndromeM Li, C Shuman, Y L Fei, et al.
Human Molecular Genetics|December 26, 2001
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1R Weksberg, J Nishikawa, O Caluseriu, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
Genomics|June 21, 2001
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutationsM Li, J Squire, C Shuman, et al.
Gynecologic Oncology|March 4, 2017
Corrigendum to "The sooner the better: Genetic testing following ovarian cancer diagnosis" [Gynecol. Oncol. 137 (2015) 423-429]E Fox, J McCuaig, R Demsky, et al.
European Journal of Medical Genetics|December 4, 2018
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatricsM J Szego, M S Meyn, C Shuman, et al.
Gynecologic Oncology|April 15, 2015
The sooner the better: Genetic testing following ovarian cancer diagnosisE Fox, J McCuaig, R Demsky, et al.
Clinical Genetics|July 22, 2014
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelinesJ A Anderson, R Z Hayeems, C Shuman, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Journal of Medical Ethics|November 27, 2016
Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?J A Anderson, M S Meyn, C Shuman, et al.
American Journal of Medical Genetics|July 31, 2001
GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndromeM Li, C Shuman, Y L Fei, et al.
Human Molecular Genetics|December 26, 2001
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1R Weksberg, J Nishikawa, O Caluseriu, et al.
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