Mosaic trisomy 1q: The longest surviving case
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32959/fullpdf
Reference16 articles.
1. Dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes;Alfaro;Leuk Res,2007
2. Trisomy 1q in a patient with severe aplastic anemia;Angelidis;Cancer Genet Cytogenet,2006
3. Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes;Christiansen;Pediatr Dev Pathol,2005
4. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born;Fernandez-Novoa;Prenat Diagn,2004
5. The common features of patients with partial trisomy of the long arm of chromosome 1;Gfatter;Clin Genet,1998
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1. Do specific ultrasonography features identified at the time of early pregnancy loss predict fetal chromosomal abnormality? – A systematic review and meta-analysis;Genes & Diseases;2019-06
2. Somatic mosaicism and neurodevelopmental disease;Nature Neuroscience;2018-10-22
3. Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype;Prenatal Diagnosis;2017-05-23
4. De NovoTrisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies;Case Reports in Genetics;2016
5. A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism;Korean Journal of Pediatrics;2016
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