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Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|September 4, 2009
Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory settingAmy M Breman, Wei-min Bi, Sau Wai Cheung
Prenatal Diagnosis|August 2, 2025
International Society for Prenatal Diagnosis 2024 Debate 3-Cytogenetics Is a Dinosaur and Should Be Replaced by Molecular TechnologiesYassmine M N Akkari, Michael E Talkowski, Amy M Breman
American Journal of Medical Genetics. Part A|June 12, 2016
4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regionsWeimin Bi, Sau-Wai Cheung, Amy M Breman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 7, 2007
Input DNA ratio determines copy number of the 33 kb Factor IX gene on de novo human artificial chromosomesAmy M Breman, Camie M Steiner, Roger B Slee, et al.
Cytogenetic and Genome Research|February 3, 2021
Two Patients with Complex Rearrangements Suggestive of Germline ChromoanagenesisPriyanka Arya, Jennelle C Hodge, Peggy A Matlock, et al.
American Journal of Medical Genetics. Part A|November 15, 2015
Triploidy mosaicism (45,X/68,XX) in an infant presenting with failure to thriveJennifer E Posey, Nikki Mohrbacher, Janice L Smith, et al.
Clinical Case Reports|November 23, 2022
A 9.8 Mb deletion at 7q31.2q31.31 downstream of <i>FOXP2</i> in an individual with speech and language impairment suggests a possible positional effectAiko Iwata-Otsubo, Victoria H Klee, Aaliya A Ahmad, et al.
Cytogenetic and Genome Research|February 9, 2022
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 DuplicationSidrah A Badar, Amy M Breman, Celanie K Christensen, et al.
Prenatal Diagnosis|January 24, 2026
Diagnosed After Birth-But Detectable Before? A Cohort Study of Prenatal Testing PotentialAllison Schartman, Olivia Woods, Leah Wetherill, et al.
European Journal of Medical Genetics|October 27, 2019
An adult female with 5q34-q35.2 deletion: A rare syndromic presentation of left ventricular non-compaction and congenital heart diseasePriyanka Arya, Theodore E Wilson, John J Parent, et al.
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