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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 dysmorphology
Feras 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-1
Morteza 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 delay
Morteza 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 rearrangements
Trilochan 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 laboratory
Arturo 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 utility
Jia-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 pandemic
Amara Z Fazal, Olivia L McGovern, Garrett W Mahon, et al.
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of 2
Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
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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 dysmorphology
Feras 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-1
Morteza 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 delay
Morteza 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 rearrangements
Trilochan 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 laboratory
Arturo 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 utility
Jia-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 pandemic
Amara Z Fazal, Olivia L McGovern, Garrett W Mahon, et al.
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of 2