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Showing results (311-320 of 388) with videos related to

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Prenatal Diagnosis|April 1, 1996
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismS L Christian, A C Smith, M Macha, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Shared and distinct phenotypic profiles among neurodevelopmental disorder genesHermela Shimelis, Matthew T Oetjens, Bobbi McGivern, et al.
The New England Journal of Medicine|March 9, 1989
The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalitiesG G Rhoads, L G Jackson, S E Schlesselman, et al.
Science (New York, N.Y.)|April 14, 1989
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomasS J Baker, E R Fearon, J M Nigro, et al.
JAMA Psychiatry|July 23, 2020
Identification of Neuropsychiatric Copy Number Variants in a Health Care System PopulationChrista Lese Martin, Karen E Wain, Matthew T Oetjens, et al.
Plos One|November 12, 2020
Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patientsMatthew T Oetjens, Jonathan Z Luo, Alexander Chang, et al.
Human Molecular Genetics|July 7, 2011
Diverse mutational mechanisms cause pathogenic subtelomeric rearrangementsYue Luo, Karen E Hermetz, Jodi M Jackson, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 30, 2020
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriersCaitlin M Hudac, Joanna Bove, Shelley Barber, et al.
American Journal of Human Genetics|May 4, 2020
Insufficient Evidence for "Autism-Specific" GenesScott M Myers, Thomas D Challman, Raphael Bernier, et al.
Pageof 39

Showing results (311-320 of 388) with videos related to

Sort By:
Pageof 39
Prenatal Diagnosis|April 1, 1996
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismS L Christian, A C Smith, M Macha, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Shared and distinct phenotypic profiles among neurodevelopmental disorder genesHermela Shimelis, Matthew T Oetjens, Bobbi McGivern, et al.
The New England Journal of Medicine|March 9, 1989
The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalitiesG G Rhoads, L G Jackson, S E Schlesselman, et al.
Science (New York, N.Y.)|April 14, 1989
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomasS J Baker, E R Fearon, J M Nigro, et al.
JAMA Psychiatry|July 23, 2020
Identification of Neuropsychiatric Copy Number Variants in a Health Care System PopulationChrista Lese Martin, Karen E Wain, Matthew T Oetjens, et al.
Plos One|November 12, 2020
Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patientsMatthew T Oetjens, Jonathan Z Luo, Alexander Chang, et al.
Human Molecular Genetics|July 7, 2011
Diverse mutational mechanisms cause pathogenic subtelomeric rearrangementsYue Luo, Karen E Hermetz, Jodi M Jackson, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 30, 2020
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriersCaitlin M Hudac, Joanna Bove, Shelley Barber, et al.
American Journal of Human Genetics|May 4, 2020
Insufficient Evidence for "Autism-Specific" GenesScott M Myers, Thomas D Challman, Raphael Bernier, et al.
Pageof 39