Increased fetal nuchal fold leading to prenatal diagnosis of ring chromosome 15
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference14 articles.
1. Two patients with ring chromosome 15 syndrome
2. Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis
3. In vitroandin vivoresponses to short-term recombinant human insulin-like growth factor-1 (IGF-I) in a severely growth-retarded girl with ring chromosome 15 and deletion of a single allele for the type 1 IGF receptor gene
4. Ring chromosome 15 syndrome
5. Fetal nuchal translucency: ultrasound screening for fetal trisomy in the first trimester of pregnancy
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1. Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review;Diagnostics;2022-04-01
2. Rare pathology derived from a ring chromosome 15. Clinical, genomic and protein interactome of genes associated with the phenotype;Bionatura;2022-02-15
3. The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review;Molecular Genetics & Genomic Medicine;2021-11-08
4. Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature;Journal of Medical Case Reports;2018-11-16
5. Recurrent enlarged nuchal translucency: First trimester presentation of a familial 15q26→qter deletion;American Journal of Medical Genetics Part A;2015-02-18
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