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Stephen W Scherer

Showing results (91-100 of 499) with videos related to

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Genome Biology|April 19, 2003
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequenceJoseph Cheung, Xavier Estivill, Razi Khaja, et al.
Scientific Reports|December 8, 2017
Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjectsIván de Jesús Ascencio-Montiel, Dalila Pinto, Esteban J Parra, et al.
Molecular Genetics & Genomic Medicine|October 20, 2021
Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testingIskra Peltekova, Afiqah Yusuf, Jennifer Frei, et al.
Journal of Genetic Counseling|September 7, 2020
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditionsAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
BMC Medical Genetics|May 8, 2020
Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerAnna Bobyn, Mehdi Zarrei, Yuankun Zhu, et al.
Diabetes|March 29, 2005
Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics StudyAndrew P Boright, Andrew D Paterson, Lucia Mirea, et al.
Cancer Letters|December 13, 2003
Chromosome 7q31 allelic imbalance and somatic mutations of RAY1/ST7 gene in colorectal cancerRiad Haddad, John B Vincent, Robert Gryfe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 27, 2004
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probandsJohn B Vincent, Debbie Kolozsvari, Wendy S Roberts, et al.
Human Mutation|September 1, 2005
Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genesLeonarda Ianzano, Junjun Zhang, Elayne M Chan, et al.
G3 (Bethesda, Md.)|February 14, 2018
Genomic Context Analysis of <i>de Novo STXBP1</i> Mutations Identifies Evidence of Splice Site DNA-Motif Associated HotspotsMohammed Uddin, Marc Woodbury-Smith, Ada J S Chan, et al.
Pageof 50

Showing results (91-100 of 499) with videos related to

Sort By:
Pageof 50
Genome Biology|April 19, 2003
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequenceJoseph Cheung, Xavier Estivill, Razi Khaja, et al.
Scientific Reports|December 8, 2017
Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjectsIván de Jesús Ascencio-Montiel, Dalila Pinto, Esteban J Parra, et al.
Molecular Genetics & Genomic Medicine|October 20, 2021
Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testingIskra Peltekova, Afiqah Yusuf, Jennifer Frei, et al.
Journal of Genetic Counseling|September 7, 2020
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditionsAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
BMC Medical Genetics|May 8, 2020
Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerAnna Bobyn, Mehdi Zarrei, Yuankun Zhu, et al.
Diabetes|March 29, 2005
Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics StudyAndrew P Boright, Andrew D Paterson, Lucia Mirea, et al.
Cancer Letters|December 13, 2003
Chromosome 7q31 allelic imbalance and somatic mutations of RAY1/ST7 gene in colorectal cancerRiad Haddad, John B Vincent, Robert Gryfe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 27, 2004
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probandsJohn B Vincent, Debbie Kolozsvari, Wendy S Roberts, et al.
Human Mutation|September 1, 2005
Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genesLeonarda Ianzano, Junjun Zhang, Elayne M Chan, et al.
G3 (Bethesda, Md.)|February 14, 2018
Genomic Context Analysis of <i>de Novo STXBP1</i> Mutations Identifies Evidence of Splice Site DNA-Motif Associated HotspotsMohammed Uddin, Marc Woodbury-Smith, Ada J S Chan, et al.
Pageof 50