Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2-Reference-Cited by-同舟云学术

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2

Published:2007-12-01 Issue:23 Volume:143A Page:2768-2774
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Khaliq Shagufta,Abid Aiysha,White Dominick R.A.,Johnson Colin A.,Ismail Muhammad,Khan Ayesha,Ayub Qasim,Sultana Salma,Maher Eamonn R.,Mehdi Syed Qasim

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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3. The ciliopathies: An emerging class of human genetic disorders;Badano;Annu Rev Genomics Hum Genet,2006

4. Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14;Brown;Arch Ophthalmol,1995

5. Autosomal recessive vitreoretinopathy and encephaloceles;Cook;Am J Ophthalmol,1982

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