Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference31 articles.
1. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation
2. A male infant with holoprosencephaly, associated with ring chromosome 21
3. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings.
4. Fetal Holoprosencephaly: Associated Malformations and Chromosomal Defects
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1. Genotype-Phenotype Analysis of 8q24.3 Duplication and 21q22.3 Deletion in a Chinese Patient and Literature Review;Public Health Genomics;2021
2. A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay;American Journal of Medical Genetics Part A;2014-01-23
3. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3;Taiwanese Journal of Obstetrics and Gynecology;2012-03
4. Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22;American Journal of Medical Genetics Part A;2011-06-10
5. Unbalanced reciprocal translocations at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2011-03
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