Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference14 articles.
1. Prenatal diagnosis of Nager syndrome in a monochorionic-diamniotic twin pregnancy;Ansart-Franquet;Prenat. Diagn.,2009
2. Sonograohy of nager Acorfascal dysostosis syndrome in utero;Benson;J. Ultrasound Med.,1988
3. Haploinsuffiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes nager syndrome;Bernier;AJHG,2012
4. A 22-week-old fetus with Nager syndrome and a congenital diaphragmatic Hernia due to a novel SF3B4 mutation;Castori;Mol. Syndromol.,2014
5. Prenatal sonographic diagnosis of Nager acrofascial dysostosis with unilateral upper limb involvement;Couyoumjian;Prenat. Diagn.,2008
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