Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome
Author:
Affiliation:
1. Department of Obstetrics and Gynecology; AP-HP, Robert Debré Hospital; Paris; France
2. Department of Developmental Biology, AP-HP; Robert Debré Hospital; Paris; France
Publisher
Wiley
Subject
Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/uog.12285/fullpdf
Reference7 articles.
1. Six cases of de Lange's syndrome; parental consanguinity in two;Pearce;Med J Aust,1967
2. The Brachmann-de Lange syndrome;Opitz;Am J Med Genet,1985
3. NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations;Gillis;Am J Hum Genet,2004
4. Lange syndrome: a clinical review of 310 individuals;Jackson;Am J Med Genet,1993
5. Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): a review of 53 CdLS pregnancies;Clark;Am J Med Genet A,2012
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