(Q80483052)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

review article

1 reference

title

[Genetic examination in cases of congenital cataract] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

B Lorenz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

publication date

1 July 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

104

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

559-565

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17571268%20AND%20SRC:MED&resulttype=core&format=json

Aetiology of childhood cataract in south India

31 December 2019

cites work

1 reference

12 December 2020

Aetiology of congenital and paediatric cataract in an Australian population

1 reference

12 December 2020

A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.

1 reference

12 December 2020

A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

1 reference

12 December 2020

Genetic origins of cataract

1 reference

12 December 2020

The genetics of childhood cataract

1 reference

12 December 2020

Congenital and infantile cataract in the United Kingdom: underlying or associated factors. British Congenital Cataract Interest Group

1 reference

12 December 2020

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations

1 reference

12 December 2020

Epidemiology of cataract in childhood: A global perspective

1 reference

12 December 2020

Measuring and interpreting the incidence of congenital ocular anomalies: lessons from a national study of congenital cataract in the UK.

1 reference

12 December 2020

Infantile cataract in the collaborative perinatal project: prevalence and risk factors

1 reference

12 December 2020

Molecular genetics of cataract

1 reference

12 December 2020

Partial sight and blindness in children of the 1970 birth cohort at 10 years of age

1 reference

12 December 2020

Genetic risk assessment

1 reference

12 December 2020

Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.

1 reference

12 December 2020

Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36

1 reference

12 December 2020

Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

1 reference

12 December 2020

A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family

1 reference

12 December 2020

Molecular genetic basis of inherited cataract and associated phenotypes

1 reference

12 December 2020

Lenticular opacities in carriers of Lowe's syndrome

1 reference

12 December 2020

CRYBA4, a novel human cataract gene, is also involved in microphthalmia

1 reference

12 December 2020

Congenital eye malformations: clinical-epidemiological analysis of 1,124,654 consecutive births in Spain

1 reference

12 December 2020

1 reference

12 December 2020