[HTML] arvojournals.org

[HTML][HTML] CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis

S Yzer, GA Fishman, J Racine… - … & visual science, 2006 - iovs.arvojournals.org
purpose. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …
被引用次数：43 相关文章

CRB1 heterozygotes with regional retinal dysfunction: Implications for genetic testing of leber congenital amaurosis

S Yzer, GA Fishman, J Racine… - … and Visual Science, 2006 - squ.pure.elsevier.com
PURPOSE. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA.) with …
[PDF] researchgate.net

[PDF][PDF] CRB1 Heterozygotes with Regional Retinal Dysfunction: Implications for Genetic Testing of Leber Congenital Amaurosis

S Yzer, GA Fishman, J Racine… - … & Visual Science, 2006 - researchgate.net
PURPOSE. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …

CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis

S Yzer, GA Fishman, J Racine… - … & visual science, 2006 - output.eyehospital.nl
PURPOSE: To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …
[PDF] academia.edu

[PDF][PDF] CRB1 Heterozygotes with Regional Retinal Dysfunction: Implications for Genetic Testing of Leber Congenital Amaurosis

S Yzer, GA Fishman, J Racine, S Al-Zuhaibi… - … & Visual Science, 2006 - academia.edu
PURPOSE. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …
[PDF] core.ac.uk

[PDF][PDF] CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of Leber congenital amaurosis

S Yzer, GA Fishman, J Racine, S Al-Zuhaibi… - … dystrophies: genotypes & … - core.ac.uk
Objectives To test humans with heterozygous CRB1 mutations for possible clinical or
functional retinal changes and evaluate whether an LCA patient with CRB1 mutations, not …

CRB1 heterozygotes with regional retinal dysfunction: Implications for genetic testing of leber congenital amaurosis

S Yzer, GA Fishman, J Racine… - … and Visual Science, 2006 - squ.elsevierpure.com
PURPOSE. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA.) with …

CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis.

S Yzer, GA Fishman, J Racine, S Al-Zuhaibi… - … & Visual Science, 2006 - europepmc.org
Purpose To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …
[HTML] arvojournals.org

[HTML][HTML] CRB1 Heterozygotes with Regional Retinal Dysfunction: Implications for Genetic Testing of Leber Congenital Amaurosis

S Yzer, GA Fishman, J Racine… - … & Visual Science, 2006 - jov.arvojournals.org
purpose. To test human CRB1 heterozygotes for possible clinical or functional retinal
changes and to evaluate whether a patient with Leber congenital amaurosis (LCA) with …
[PDF] ru.nl

[PDF][PDF] CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of Leber congenital amaurosis

S Yzer, GA Fishman, J Racine, S Al-Zuhaibi… - Autosomal recessive … - repository.ubn.ru.nl
Objectives To test humans with heterozygous CRB1 mutations for possible clinical or
functional retinal changes and evaluate whether an LCA patient with CRB1 mutations, not …