Congenital diaphragmatic hernia: Is 15q26.1-26.2 a candidate locus?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference23 articles.
1. Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)
2. Diaphragm defects occur in a CDH hernia model independently of myogenesis and lung formation
3. Sonographic detection of fetuses with trisomies 13 and 18: Accuracy and limitations
4. Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo)
5. 2000. Diaphragmatic hernia. Fetology. New York: McGraw-Hill. pp 299-311.
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2. Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic Hernia;European Journal of Pediatric Surgery;2021-12
3. Expanding the clinical spectrum of pathogenic variation in NR2F2: Asplenia;European Journal of Medical Genetics;2021-12
4. 15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review;Italian Journal of Pediatrics;2021-09-16
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