Ectopia lentis as the presenting and primary feature in Marfan syndrome-Reference-Cited by-同舟云学术

Ectopia lentis as the presenting and primary feature in Marfan syndrome

Published:2011-09-19 Issue:11 Volume:155 Page:2661-2668
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zadeh Neda,Bernstein Jonathan A.,Niemi Anna Kaisa,Dugan Sarah,Kwan Andrea,Liang David,Hyland James C.,Hoyme H. Eugene,Hudgins Louanne,Manning Melanie A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

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3. A novel de novo mutation in exon 14 of the fibrillin-1 gene associated with delayed secretion of fibrillin in a patient with a mild Marfan phenotype;Booms;Hum Genet,1997

4. Marfan database (third edition): New mutations and new routines for the software;Collod-Beroud;Nucl Acids Res,1998

5. Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus;Comeglio;Br J Ophthalmol,2002

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