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W Mahon

Showing results (11-20 of 17) with videos related to

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Journal of Pediatric Genetics|September 15, 2016
Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphologyFeras M Hantash, Boris T Wang, Renius Owen, et al.
Molecular Cytogenetics|September 8, 2017
CMA analysis identifies homozygous deletion of <i>MCPH1</i> in 2 brothers with primary Microcephaly-1Morteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Molecular Cytogenetics|December 6, 2014
Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delayMorteza Hemmat, Xiaojing Yang, Patricia Chan, et al.
European Journal of Human Genetics : EJHG|April 10, 2014
Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangementsTrilochan Sahoo, Jia-Chi Wang, Mohamed M Elnaggar, et al.
Molecular Cytogenetics|January 18, 2012
Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratoryArturo Anguiano, Boris T Wang, Shirong R Wang, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utilityJia-Chi Wang, Leslie Ross, Loretta W Mahon, et al.
Antimicrobial Stewardship & Healthcare Epidemiology : ASHE|June 26, 2025
Trends in inpatient antibiotic use in Indonesia and the Philippines during the COVID-19 pandemicAmara Z Fazal, Olivia L McGovern, Garrett W Mahon, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Journal of Pediatric Genetics|September 15, 2016
Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphologyFeras M Hantash, Boris T Wang, Renius Owen, et al.
Molecular Cytogenetics|September 8, 2017
CMA analysis identifies homozygous deletion of <i>MCPH1</i> in 2 brothers with primary Microcephaly-1Morteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Molecular Cytogenetics|December 6, 2014
Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delayMorteza Hemmat, Xiaojing Yang, Patricia Chan, et al.
European Journal of Human Genetics : EJHG|April 10, 2014
Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangementsTrilochan Sahoo, Jia-Chi Wang, Mohamed M Elnaggar, et al.
Molecular Cytogenetics|January 18, 2012
Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratoryArturo Anguiano, Boris T Wang, Shirong R Wang, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utilityJia-Chi Wang, Leslie Ross, Loretta W Mahon, et al.
Antimicrobial Stewardship & Healthcare Epidemiology : ASHE|June 26, 2025
Trends in inpatient antibiotic use in Indonesia and the Philippines during the COVID-19 pandemicAmara Z Fazal, Olivia L McGovern, Garrett W Mahon, et al.
Pageof 2