(Q73875054)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

P Watts

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Rees

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Clarke

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

L Beck

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

C Lane

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M J Owen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

J Gray

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 April 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

14 ( Pt 2)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

172-175

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10845011%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/eye.2000.48

7 November 2019

exact match

0 references

cites work

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

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7 January 2021

https://api.crossref.org/works/10.1038%2FEYE.2000.48

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7 January 2021

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7 January 2021

Autosomal dominant congenital cataract. Morphology and genetic mapping

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

The genetics of cataract: our vision becomes clearer

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Activation of the gamma E-crystallin pseudogene in the human hereditary Coppock-like cataract.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A progressive early onset cataract gene maps to human chromosome 17q24.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Connexin46 mutations in autosomal dominant congenital cataract

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Autosomal dominant congenital cataract. Interocular phenotypic variability.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A new locus for dominant "zonular pulverulent" cataract, on chromosome 13

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Physiological properties of the normal lens

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

PROBABLE LINKAGE BETWEEN A CONGENITAL CATARACT LOCUS AND THE DUFFY BLOOD GROUP LOCUS

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A locus for autosomal dominant posterior polar cataract on chromosome 1p

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021

A locus for autosomal dominant anterior polar cataract on chromosome 17p

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2000.48

7 January 2021