Molecular cytogenetic characterization of an inherited maternal duplication 20p11.21p13 associated with a small 20p11.21 deletion
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33741/fullpdf
Reference12 articles.
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2. De novo trisomy 20p of paternal origin;Chaabouni;Am J Med Genet Part A,2007
3. Identification of a novel glial cell line-derived neurotrophic factor-inducible gene required for renal branching morphogenesis;Fukuda;J Biol Chem,2003
4. Hippocampal SSTR4 somatostatin receptors control the selection of memory strategies;Gastambide;Psychopharmacology,2009
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1. Clinical Observation of a Child with Prenatally Diagnosed De Novo Partial Trisomy of Chromosome 20;Fetal and Pediatric Pathology;2019-03-20
2. Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements;Molecular Cytogenetics;2016-01-28
3. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services;Gene;2014-02
4. Combined immunodeficiency in a 3-year-old boy with 16p11.2 and 20p12.2-11.2 chromosomal duplications;American Journal of Medical Genetics Part A;2013-12-05
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