(Q35248941)

7 August 2017

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning (English)

1 reference

7 August 2017

F Mirzayans

1

1 reference

7 August 2017

A J Mears

2

1 reference

7 August 2017

S W Guo

3

1 reference

7 August 2017

W G Pearce

4

1 reference

7 August 2017

M A Walter

5

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 July 1997

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

61

1 reference

7 August 2017

111-119

1 reference

7 August 2017

1

1 reference

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Genomic mismatch scanning: a new approach to genetic linkage mapping

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Limits of resolution of genetic linkage studies: implications for the positional cloning of human disease genes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Genomic mismatch scanning: current progress and potential applications

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Proportion of genome shared identical by descent by relatives: concept, computation, and applications

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Mutation of the PAX6 gene in patients with autosomal dominant keratitis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Familial hypoplasia of the iris stroma associated with glaucoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Genomic analysis II: isolation of high molecular weight heteroduplex DNA following differential methylase protection and Formamide-PERT hybridization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Accurate and superaccurate gene mapping

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715869

Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree

27 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9245991

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autosomal dominant iridogoniodysgenesis: genetic features

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9245991

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/513894

1 reference

7 August 2017

1 reference

7 August 2017

1 reference