Chromosomal microarray analysis as a first‐tier clinical diagnostic test: Estonian experience - Žilina - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes - ScienceDirect
Genetics of 15q Duplications - Dup15Q Alliance
A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: Molecular characterization of the marker - ScienceDirect
AHS Genetic Testing 2019 - Genome Sequencing Blog For Everyday People | Merogenomics Inc.
![A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]](https://dfzljdn9uc3pi.cloudfront.net/2014/354/1/fig-2-full.png "A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]")
A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]
Cytogenetic Abnormalities
![A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]](https://dfzljdn9uc3pi.cloudfront.net/2014/354/1/fig-1-2x.jpg "A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]")
A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings [PeerJ]
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders | PLOS Genetics
Genetic Analysis of Copy Number Variation in Large Chorangiomas - Meeli Sirotkina, Konstantinos Douroudis, Magnus Westgren, Nikos Papadogiannakis, 2019
Genetics of 15q Duplications - Dup15Q Alliance
AHS Genetic Testing 2019 - Genome Sequencing Blog For Everyday People | Merogenomics Inc.
The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature - Urraca - 2013 - Autism Research - Wiley Online Library
Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases - ScienceDirect
Genetics of 15q Duplications - Dup15Q Alliance
15q11.2 Microduplications
15q11-q13 duplication syndrome: MedlinePlus Genetics
SciELO - Brasil - Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report
Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1 | Leukemia
Frontiers | A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism
PDF) Prieto P, Ramirez C, Cabrera A, Ballesteros J, and A Martín. 2005. Development and cytogenetic characterization of non-brittle rachis tritordeum lines. Chromosome Research 109 (1-3):145 | Pilar Prieto - Academia.edu
Chromosomes 15 and 22: deletions and inverted duplication chromosomes | Learn Science at Scitable
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders | PLOS Genetics
15q11-q13 duplication syndrome: MedlinePlus Genetics
CNVs in chromosome 2q11.1–2q13. Minimum CNV sizes are represented by... | Download Scientific Diagram
