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Showing results (711-720 of 729) with videos related to

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Physical Review Letters|November 9, 2019
Multiple Shape Coexistence in ^{110,112}CdP E Garrett, T R Rodríguez, A Diaz Varela, et al.
American Journal of Human Genetics|July 10, 2012
Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomaliesHyung-Goo Kim, Hyun-Taek Kim, Natalia T Leach, et al.
American Journal of Human Genetics|November 5, 2019
Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent MiscarriageZirui Dong, Junhao Yan, Fengping Xu, et al.
American Journal of Human Genetics|March 6, 2008
Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy projectAnne W Higgins, Fowzan S Alkuraya, Amy F Bosco, et al.
American Journal of Respiratory and Critical Care Medicine|September 23, 2025
Airway Epithelial Heterogeneity and Mucus Plugging in Asthmatic BronchiolesStephen A Schworer, Hiroaki Murano, Hong Dang, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative studyP S Ing, D L Van Dyke, S P Caudill, et al.
Nature Communications|October 26, 2019
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisC S Gallagher, N Mäkinen, H R Harris, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
Human Reproduction (Oxford, England)|December 5, 2023
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundityHamdi Mbarek, Scott D Gordon, David L Duffy, et al.
Pageof 73

Showing results (711-720 of 729) with videos related to

Sort By:
Pageof 73
Physical Review Letters|November 9, 2019
Multiple Shape Coexistence in ^{110,112}CdP E Garrett, T R Rodríguez, A Diaz Varela, et al.
American Journal of Human Genetics|July 10, 2012
Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomaliesHyung-Goo Kim, Hyun-Taek Kim, Natalia T Leach, et al.
American Journal of Human Genetics|November 5, 2019
Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent MiscarriageZirui Dong, Junhao Yan, Fengping Xu, et al.
American Journal of Human Genetics|March 6, 2008
Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy projectAnne W Higgins, Fowzan S Alkuraya, Amy F Bosco, et al.
American Journal of Respiratory and Critical Care Medicine|September 23, 2025
Airway Epithelial Heterogeneity and Mucus Plugging in Asthmatic BronchiolesStephen A Schworer, Hiroaki Murano, Hong Dang, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative studyP S Ing, D L Van Dyke, S P Caudill, et al.
Nature Communications|October 26, 2019
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisC S Gallagher, N Mäkinen, H R Harris, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
Human Reproduction (Oxford, England)|December 5, 2023
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundityHamdi Mbarek, Scott D Gordon, David L Duffy, et al.
Pageof 73