Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental field
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03108.x/fullpdf
Reference19 articles.
1. Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome;Bamforth;Am. J. Med. Genet.,1989
2. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2;Clark;Am. J. Med. Genet.,1989
3. Schisis-association;Czeizel;Am. J. Med. Genet.,1981
4. Ring chromosome 15 in a patient with features of Fryns syndrome;Jong;J. Med. Genet.,1989
5. Absent left hemidiaphragm, arrhinencephaly, and cardiac malformations;Fitch;J. Med. Genet.,1978
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1. Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review;Frontiers in Genetics;2021-06-07
2. Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome;Clinical Genetics;2008-06-28
3. Dandy–Walker syndrome and chromosomal abnormalities;Congenital Anomalies;2007-12
4. Genetic Factors in Congenital Diaphragmatic Hernia;The American Journal of Human Genetics;2007-05
5. Cardiovascular malformations in Fryns syndrome: Is there a pathogenic role for neural crest cells?;American Journal of Medical Genetics Part A;2005
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