A rare case of aniridia and balanced translocation (5:11)(p15.3;q22) arising in the same subject: et challenge for genetic counseling: The authors report on a case of isolated aniridia caused by haploinsufficiency of the PAX6 gene, which is located on 11p13, and a balanced translocation t(5;11)(p15.3;q22) inherited respectively from his father and his mother. Due to the coincidence of two abnormalities in the same chromosome, the segregation of the mutant allele leading to aniridia and of the chromosomes involved in the translocation are not independent events. Considering that both monosomy and trisomy for 11q22-qter are unviable, his offspring may inherit either the PAX6 mutation or the balanced translocation. However, depending on the oc...
Background Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a se...
<p><b>Purpose</b>: Congenital aniridia, a severe bilateral panocular visual disorder, is an autosoma...
PURPOSE: PAX6 mutations cause aniridia as well as other various congenital eye abnormalities. Aniri...
A series of 125 patients referred primarily with aniridia classified as either sporadic (74), famili...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
We report two novel PAX6 mutations in aniridia patients of two Swiss pedigrees (We, Sc) which give r...
<p>Non-syndromic aniridia (iris hypoplasia) as an autosomal dominant eye disorder results from the c...
A two-year-old boy presenting with bilateral aniridia and psychomotor retardation had a de novo (2;3...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
Contains fulltext : 69203.pdf (publisher's version ) (Closed access)Two female neo...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
Purpose: To identify a disease-causing paired box 6 (PAX6) gene mutation in a Chinese family affecte...
Background Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a se...
<p><b>Purpose</b>: Congenital aniridia, a severe bilateral panocular visual disorder, is an autosoma...
PURPOSE: PAX6 mutations cause aniridia as well as other various congenital eye abnormalities. Aniri...
A series of 125 patients referred primarily with aniridia classified as either sporadic (74), famili...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
We report two novel PAX6 mutations in aniridia patients of two Swiss pedigrees (We, Sc) which give r...
<p>Non-syndromic aniridia (iris hypoplasia) as an autosomal dominant eye disorder results from the c...
A two-year-old boy presenting with bilateral aniridia and psychomotor retardation had a de novo (2;3...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
Contains fulltext : 69203.pdf (publisher's version ) (Closed access)Two female neo...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
We report molecular genetic analysis of 42 affected individuals referred with a diagnosis of aniridi...
Purpose: To identify a disease-causing paired box 6 (PAX6) gene mutation in a Chinese family affecte...
Background Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a se...
<p><b>Purpose</b>: Congenital aniridia, a severe bilateral panocular visual disorder, is an autosoma...
PURPOSE: PAX6 mutations cause aniridia as well as other various congenital eye abnormalities. Aniri...