Different Cardiac Anomalies in Mother and Son with 4q-Syndrome
Author:
Affiliation:
1. Cardiology Department, Ospedali Riuniti Villa Sofia Cervello, 90100 Palermo, Italy
2. Pediatric Clinic, Policlinico Universitario, Palermo, Italy
Abstract
Publisher
Hindawi Limited
Subject
General Medicine
Link
http://downloads.hindawi.com/journals/crig/2015/932651.pdf
Reference12 articles.
1. The spectrum of 4q- syndrome illustrated by a case series
2. Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
3. Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene
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1. Clinical comparison between terminal and interstitial 4q deletion in two unrelated children;2022-10-10
2. Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype;Open Life Sciences;2022-01-01
3. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder;Molecular Cytogenetics;2021-09-04
4. SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients;eLife;2021-06-08
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