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Ian A Glass

Showing results (1-10 of 119) with videos related to

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Current Opinion in Cardiology|April 21, 2004
Genotype-phenotype correlation in congenital heart diseaseMark B Lewin, Ian A Glass, Patricia Power
European Journal of Medical Genetics|February 8, 2006
Double aneuploidy (48,XXY,+21): molecular analysis demonstrates a maternal originIan A Glass, Lei Li, Philip D Cotter
European Journal of Human Genetics : EJHG|March 23, 2007
Joubert syndrome (and related disorders) (OMIM 213300)Melissa A Parisi, Dan Doherty, Phillip F Chance, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 28, 2018
Minimal mosaicism, maximal phenotype: Discordance between clinical and molecular findings in two patients with tuberous sclerosisHeather M Byers, Dana M Jensen, Ian A Glass, et al.
Pediatric Cardiology|July 11, 2006
Aortic root dilatation is a rare complication of Noonan syndromePatricia D Power, Mark B Lewin, Mark C Hannibal, et al.
Bio-Protocol|March 20, 2020
Laser Capture Micro-dissection (LCM) of Neonatal Mouse Forebrain for RNA IsolationAchira Roy, Mei Deng, Kimberly A Aldinger, et al.
Frontiers in Physiology|April 1, 2017
Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from MiceKai Yu, Mei Deng, Theresa Naluai-Cecchini, et al.
Pediatric Cardiology|March 14, 2024
Differential Regulation of Immune-Related Genes in the Developing HeartMathieu Garand, Susie S Y Huang, Brian Dineen, et al.
Epilepsia|January 9, 2009
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patientsCraig L Bennett, Yingzhang Chen, Sihoun Hahn, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisionsHeather M Byers, Maida Chen, Andrew S Gelfand, et al.
Pageof 12

Showing results (1-10 of 119) with videos related to

Sort By:
Pageof 12
Current Opinion in Cardiology|April 21, 2004
Genotype-phenotype correlation in congenital heart diseaseMark B Lewin, Ian A Glass, Patricia Power
European Journal of Medical Genetics|February 8, 2006
Double aneuploidy (48,XXY,+21): molecular analysis demonstrates a maternal originIan A Glass, Lei Li, Philip D Cotter
European Journal of Human Genetics : EJHG|March 23, 2007
Joubert syndrome (and related disorders) (OMIM 213300)Melissa A Parisi, Dan Doherty, Phillip F Chance, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 28, 2018
Minimal mosaicism, maximal phenotype: Discordance between clinical and molecular findings in two patients with tuberous sclerosisHeather M Byers, Dana M Jensen, Ian A Glass, et al.
Pediatric Cardiology|July 11, 2006
Aortic root dilatation is a rare complication of Noonan syndromePatricia D Power, Mark B Lewin, Mark C Hannibal, et al.
Bio-Protocol|March 20, 2020
Laser Capture Micro-dissection (LCM) of Neonatal Mouse Forebrain for RNA IsolationAchira Roy, Mei Deng, Kimberly A Aldinger, et al.
Frontiers in Physiology|April 1, 2017
Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from MiceKai Yu, Mei Deng, Theresa Naluai-Cecchini, et al.
Pediatric Cardiology|March 14, 2024
Differential Regulation of Immune-Related Genes in the Developing HeartMathieu Garand, Susie S Y Huang, Brian Dineen, et al.
Epilepsia|January 9, 2009
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patientsCraig L Bennett, Yingzhang Chen, Sihoun Hahn, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisionsHeather M Byers, Maida Chen, Andrew S Gelfand, et al.
Pageof 12