Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols-Reference-Cited by-同舟云学术

Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols

Published:2009-07-16 Issue:10 Volume:29 Page:966-974
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Langlois Sylvie,Armstrong Linlea,Gall Kim,Hulait Gurdip,Livingston Janet,Nelson Tanya,Power Patricia,Pugash Denise,Siciliano Dawn,Steinraths Michelle,Mattman André

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2326/fullpdf

Reference33 articles.

1. Unconjugated estriol as an indication for prenatal diagnosis of steroid sulfatase deficiency by in situ hybridization;Ahmed;Obstet Gynecol,1998

2. Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques;Aviram-Goldring;Int J Dermatol,2000

3. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome;Ballabio;Proc Natl Acad Sci U.S.A.,1989

4. Prenatal detection of X-linked ichthyosis by maternal serum screening for Down syndrome;Bartels;Prenat Diagn,1994

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