Vasomotor instability in neonates with chromosome 22q11 deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference30 articles.
1. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
2. 1994. Cardiac surgery of the neonate and infant. Philadelphia: WB Saunders. 514 p.
3. Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization
4. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
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2. 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects;Children;2022-05-25
3. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022
4. Performance of a targeted cell‐free DNA prenatal test for 22q11.2 deletion in a large clinical cohort;Ultrasound in Obstetrics & Gynecology;2021-10
5. Asymmetric crying facies – its meaning in the differential diagnosis of congenital developmental abnormalities;Medical Studies;2019
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