Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: A specific cardiac phenotype associated with deletion 18q syndrome-Reference-Cited by-同舟云学术

Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: A specific cardiac phenotype associated with deletion 18q syndrome

Published:2005 Issue:2 Volume:138A Page:185-186
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Versacci Paolo,Digilio M. Cristina,Sauer Ursula,Dallapiccola Bruno,Marino Bruno

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: A 6-year prospective study

2. Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q

3. “Agenesis” of ductus arteriosus associated with the syndrome of tetralogy of fallot and absent pulmonary valve

4. , , . 1997. Genetic and environmental risk factors of major cardiovascular malformations. The Baltimore-Washington Infant Study 1981-1989. Armonk, New York: Futura Publishing Company, Inc. p 227-265.

5. Absent pulmonary valve syndrome with intact ventricular septum and patent ductus arteriosus: report of two cases and a short review of the literature

Cited by 24 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. Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness;Clinical Genetics;2023-07-17

2. Pulmonary artery sling in a 22‐month‐old boy with 18q deletion syndrome: A rare but possible association;Echocardiography;2022-04-17

3. Increased Diagnostic Yield of Array Comparative Genomic Hybridization for Autism Spectrum Disorder in One Institution in Taiwan;Medicina;2021-12-22

4. Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing;Frontiers in Genetics;2021-09-20

5. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects;Taiwanese Journal of Obstetrics and Gynecology;2019-09