Toriello-Carey syndrome phenotype and chromosome anomalies-Reference-Cited by-同舟云学术

Toriello-Carey syndrome phenotype and chromosome anomalies

Published:2007 Issue:1 Volume:146A Page:116-116
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Toriello Helga V.,Hatchwell Eli

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference6 articles.

1. , , , , , , , . 2007. Application of a novel tiling-path aCGH platform reveals additional genetic heterogeneity in Toriello-Carey syndrome. Presented at the American College of Medical Genetics meeting, Nashville.

2. "Molecular rulers" for calibrating phenotypic effects of telomere imbalance

3. Toriello-Carey syndrome and unbalanced translocation t(8;18)(p12;q22)

4. Toriello-Carey syndrome

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 6q13q14.3 Microdeletion Syndrome with Severe Hypotonia and Facial Dysmorphism: Genotype–Phenotype Correlation;Journal of Pediatric Genetics;2021-01-06

2. Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review;Molecular Syndromology;2017-11-29

3. Response to: Toriello et al., “Update on the Toriello-Carey Syndrome.” Further delineation of a young woman with deletion 1q42.12-q42.2;American Journal of Medical Genetics Part A;2017-04-26

4. DDX3X mutations in two girls with a phenotype overlapping Toriello–Carey syndrome;American Journal of Medical Genetics Part A;2017-03-29

5. A Chinese patient with Toriello-Carey syndrome and an interstitial deletion of 3q;American Journal of Medical Genetics Part A;2016-10-17