Gillespie syndrome phenotype withat(x;11)(p22.32;p12) de novo translocation-Reference-Cited by-同舟云学术

Gillespie syndrome phenotype withat(x;11)(p22.32;p12) de novo translocation

Published:1998-03 Issue:3 Volume:125 Page:397-399
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Dollfus Hélène,Joanny-Flinois Olivier,Doco-Fenzy Martine,Veyre Lysiane,Joanny-Flinois Lina,Khoury Maroun,JonveauxB Philippe,Abitbol Marc,Dufier Jean-Louis

Publisher

Elsevier BV

Subject

Ophthalmology

Reference5 articles.

1. Die bedeutung der atypischen kolobome und defekte der iris für dir erkennenung des hereditären aniridie-syndroms;Delleman;Klin Monatsbl Augenheilkd,1973

2. Aniridia, cerebellar ataxia and oligophrenia in siblings;Gillespie;Arch Ophthalmol,1964

3. Gillespie's syndrome;François;Ophthalmic Paediatr Genet,1983

4. The human Pax6 gene is mutated in two patients with aniridia;Jordan;Nat Genet,1992

5. Absence of Pax6 gene mutations in Gillespie syndrome;Glaser;Genomics,1994

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