Prenatal diagnosis of Pallister Killian Syndrome in a fetus with congenital diaphragmatic hernia, short limbs, and increased nuchal translucency
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference5 articles.
1. Mosaic tetrasomy 12p;Gilgenkrantz;Clin Genet,1985
2. Pallister-Killian syndrome presenting through nuchal translucency screening for trisomy 21;Langford;Prenat Diagn,2000
3. First trimester diagnosis of Pallister-Killian syndrome in a fetus with suggestive abnormalities;Mourali;Tunis Med,2010
4. Prenatal diagnosis of Pallister-Killian syndrome associated with pulmonary stenosis and right ventricular dilatation;Park;Korean J Lab Med,2009
5. Novel clinical manifestations in Pallister-Killian syndrome: comprehensive evaluation of 59 affected individuals and review of previously reported cases;Wilkens;Am J Med Genet A,2012
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1. Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic Hernia;European Journal of Pediatric Surgery;2021-12
2. Prenatal profile of Pallister-Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis;American Journal of Medical Genetics Part A;2018-10-05
3. Pallister‐Killian syndrome: Review of fetal phenotype;Clinical Genetics;2018-06-29
4. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister–Killian syndrome detected by amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2017-12
5. Targeted prenatal diagnosis of Pallister-Killian syndrome;Prenatal Diagnosis;2017-03-27
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