Essential thrombocythemia | Orphanet Journal of Rare Diseases | Full Text
Chromosome 15q11-Q13 Duplication Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders | PLOS Genetics
Frontiers | A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism
Chromosomal microarray analysis as a first‐tier clinical diagnostic test: Estonian experience - Žilina - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
PDF) De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature | Maria Tzetis, Christina Vrettou, Krinio Giannikou, and Andreas
![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]
Genetics of 15q Duplications - Dup15Q Alliance
Frontiers | A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism
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
Cytogenetic Abnormalities
The clinical diagnostic utility of array CGH in children with syndromic microcephaly Goyal M, Faruq M, Gupta A, Shrivastava D, Shamim U - Ann Indian Acad Neurol
AHS Genetic Testing 2019 - Genome Sequencing Blog For Everyday People | Merogenomics Inc.
Chromosomes 15 and 22: deletions and inverted duplication chromosomes | Learn Science at Scitable
CNVs in chromosome 2q11.1–2q13. Minimum CNV sizes are represented by... | Download Scientific Diagram
15q11.2 Microduplications
Genetics of 15q Duplications - Dup15Q Alliance
Genetics of 15q Duplications - Dup15Q Alliance
Genetics of 15q Duplications - Dup15Q Alliance
15q11-q13 duplication syndrome: MedlinePlus Genetics
Genetics of 15q Duplications - Dup15Q Alliance
AHS Genetic Testing 2019 - Genome Sequencing Blog For Everyday People | Merogenomics Inc.
