(Q40879865)

24 September 2017

1 reference

title

Molecular genetics is revolutionizing our understanding of ophthalmic disease (English)

1 reference

24 September 2017

1 reference

K F Damji

1

1 reference

PubMed ID

9323944

24 September 2017

R R Allingham

series ordinal

2

1 reference

PubMed ID

9323944

24 September 2017

language of work or name

English

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publication date

1 October 1997

1 reference

American Journal of Ophthalmology

24 September 2017

1 reference

24 September 2017

124

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24 September 2017

4

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24 September 2017

530-543

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Gene mapping of ocular diseases

24 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

The revolution in molecular genetics and its impact on ophthalmology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Molecular biology in ophthalmology. A review of principles and recent advances

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

A General Model for the Genetic Analysis of Pedigree Data

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Evolution of sickle variant gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

The polymerase chain reaction. A new method of using molecular genetics for medical diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Molecular genetics of retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Pax6: more than meets the eye.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Positional cloning moves from perditional to traditional

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Genetic dissection of complex traits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Human/mouse homology relationships

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Recent advances in the application of gene therapy to human disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Genetic discrimination and health insurance: an urgent need for reform.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Genetic and molecular studies of macular dystrophies: recent developments

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

Genetic clues to glaucoma's secrets. The L Edward Jackson Memorial Lecture. Part 2.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2970869-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(14)70869-4

1 reference

24 September 2017

1 reference

PubMed ID

9323944