PRENATAL DIAGNOSIS OF THE 22q11 DELETION SYNDROME
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference16 articles.
1. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
2. A deletion in chromosome 22 can cause digeorge syndrome
3. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
4. The association of the DiGeorge anomalad with partial monosomy of chromosome 22
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1. Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome;American Journal of Medical Genetics Part A;2018-07-28
2. La dysgénésie thymique : marqueur de microdélétion 22q11.2 dans le bilan d’un hydramnios;Journal de Gynécologie Obstétrique et Biologie de la Reproduction;2016-04
3. Molecular Cytogenetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2015-11-23
4. Postnatal Diagnosis of 22q11.2 Deletion Syndrome in Fetal Megalourethra;Journal of Ultrasound in Medicine;2015-02
5. Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases;EPMA Journal;2011-05-06
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