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Prenatal Diagnosis|July 18, 2003
Three different origins for apparent triploid/diploid mosaicsArt Daniel, Zhanhe Wu, Artur Darmanian, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomaliesArt Daniel, Artur Darmanian, Greg Peters, et al.
Prenatal Diagnosis|August 10, 2004
Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicismArt Daniel, Zhanhe Wu, Artur Darmanian, et al.
Cancer Research|February 28, 2007
Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesisElizabeth M Algar, Luke St Heaps, Artur Darmanian, et al.
Cancers|July 20, 2021
Neuroblastoma Molecular Risk-Stratification of DNA Copy Number and <i>ALK</i> Genotyping via Cell-Free Circulating Tumor DNA ProfilingSmadar Kahana-Edwin, Lucy E Cain, Geoffrey McCowage, et al.
Genetic Testing and Molecular Biomarkers|October 1, 2016
Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome AbnormalitiesDale Wright, Louise Carey, Siobhan Battersby, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalancesArt Daniel, Elizabeth Baker, Nicole Chia, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotypeCarolyn J Ellaway, Gladys Ho, Elisa Bettella, et al.
Pathology|July 6, 2023
SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratoryCon Ngo, Maria Baluyot, Bruce Bennetts, et al.
American Journal of Medical Genetics. Part A|September 16, 2023
Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autismDale Cameron Wright, Maria Lourdes Baluyot, Johanna Carmichael, et al.
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