A RARE CASE OF INTERSTITIAL del(1)(p34.3p36.11) DIAGNOSED PRENATALLY-Reference-Cited by-同舟云学术

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A RARE CASE OF INTERSTITIAL del(1)(p34.3p36.11) DIAGNOSED PRENATALLY

Published:2004-01 Issue:4 Volume:23 Page:251-255
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Yang Hua,Lee Christine L. Y.,Young David C.,Shortliffe Michelle,Yu Weiming,Wright James R.

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Deletion of chromosome 1p: a short review

2. Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality

3. Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome

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2. Fetal Cardiac Anomalies;Journal of Fetal Medicine;2018-02-19

3. Fetal Heart Size;Journal of Ultrasound in Medicine;2016-10-13

4. Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities;Molecular Cytogenetics;2016-10-06

5. Altered Z-disks of myofibrils in the cardiomyocytes from patients with Ebstein’s anomaly;Arkhiv patologii;2015

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