18p trisomy: A case of direct 18p duplication characterized by molecular cytogenetic analysis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference18 articles.
1. Partial Trisomy of Chromosome 18 (pter→q12) following a Familial 18;21 Translocation rcp(18;21)(q12;q11)
2. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion
3. Monosomy 18p and pure trisomy 18p in a family with translocation (7;18).
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1. Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies;Taiwanese Journal of Obstetrics and Gynecology;2022-05
2. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation;Ophthalmic Genetics;2020-03-03
3. Prenatal detection of interstitial 18p11.31‐p11.22 microduplications: Phenotypic diversity and literature review;Prenatal Diagnosis;2019-09-05
4. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman;Molecular Genetics & Genomic Medicine;2019-07-17
5. Two-Generation Transmission of Trisomy 18p: Prenatal Diagnosis in a Woman with Mild Intellectual Disability;Cytogenetic and Genome Research;2019
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