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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.
American Journal of Medical Genetics. Part A|May 21, 2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotypeJia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, et al.
Molecular Cytogenetics|May 4, 2013
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature reviewMorteza Hemmat, Omid Hemmat, Arturo Anguiano, et al.
Scientific Reports|February 9, 2022
Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratorySun Hee Rosenthal, Anna Gerasimova, Rolando Ruiz-Vega, et al.
Plos One|March 2, 2017
Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)Charles M Strom, Ben Anderson, David Tsao, et al.
Biomed Research International|February 25, 2020
Development and Validation of a 34-Gene Inherited Cancer Predisposition Panel Using Next-Generation SequencingSun Hee Rosenthal, Weimin Sun, Ke Zhang, et al.
Neuromuscular Disorders : NMD|October 1, 2015
Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHDJessica Vasale, Fatih Boyar, Michael Jocson, 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.
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