Prenatal diagnosis and ultrasonographic findings of partial trisomy of chromosome 6q
Author:
Funder
Department of Finance of Jilin Province
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference14 articles.
1. Three cases with de novo 6q imbalance and variable prenatal phenotype;Grati,2005
2. Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype;Marinescu;Clin Case Rep,2015
3. Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations;Cavani;Prenat Diagn,2003
4. A 15 Mb duplication of 6q24.1-q25.3 associated with typical but milder features of the duplication 6q syndrome;Zweier;Eur J Med Genet,2008
5. Interstitial 6q21q23 duplication-variant of variable phenotype and incomplete penetrance or benign duplication?;Srebniak;Mol Cytogenet,2016
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1. Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q;BMC Pediatrics;2023-11-22
2. Exome and Genome Sequencing to Unravel the Precise Breakpoints of Partial Trisomy 6q and Partial Monosomy 2q;2023-05-08
3. Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature;Journal of Autism and Developmental Disorders;2022-12-11
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