(Q35246146)

7 August 2017

Mapping of Alport syndrome to the long arm of the X chromosome (English)

1 reference

7 August 2017

1 reference

C L Atkin

1

1 reference

7 August 2017

S J Hasstedt

2

1 reference

7 August 2017

L Menlove

3

1 reference

7 August 2017

L Cannon

4

1 reference

7 August 2017

N Kirschner

5

1 reference

7 August 2017

C Schwartz

6

1 reference

7 August 2017

K Nguyen

7

1 reference

7 August 2017

M Skolnick

8

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 February 1988

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

42

1 reference

7 August 2017

249-255

1 reference

7 August 2017

2

1 reference

Abnormal Segregation in Hereditary Renal Disease with Deafness

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Partially sex-linked cominant inheritance of interstitial pyelonephritis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Sequential tests for the detection of linkage

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

A highly polymorphic locus in human DNA

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

X-linked inheritance of Alport syndrome: family P revisited

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

A strategy to reveal high-frequency RFLPs along the human X chromosome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Alport's syndrome of hereditary nephritis and deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Genetics of hereditary nephropathy with deafness (Alport's disease)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

A General Model for the Genetic Analysis of Pedigree Data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Hereditary macrothrombocytopathia, nephritis and deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Segregation Ratios in Alport's Syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

The genetic linkage map of the human X chromosome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Genetic heterogeneity among kindreds with Alport syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Goodness-of-fit tests for locus order in three-point mapping

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Alport’s Syndrome Associated with Macrothrombopathic Thrombocytopenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Apparently changing patterns of inheritance in Alport's hereditary nephritis: genetic heterogeneity versus altered diagnostic criteria.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715268

Hereditary Nephritis: A Re-examination of its Clinical and Genetic Features

26 September 2018

1 reference

12 December 2020

Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds

1 reference

12 December 2020

A clinical study of hereditary interstitial pyelonephritis

1 reference

12 December 2020

Familial hereditary nephropathy (Alport's syndrome)

1 reference

12 December 2020

Early pathologic features of hereditary nephritis: a clinicopathologic correlation

1 reference

12 December 2020

HEREDITARY RENAL DYSFUNCTION AND DEAFNESS

1 reference

12 December 2020

CONGENITAL HEREDITARY NEPHRITIS WITH NERVE DEAFNESS

1 reference

12 December 2020

Hereditary nephritis (Alport's syndrome)-1983

1 reference

12 December 2020

The genetics of the Alport syndrome

1 reference

12 December 2020

Identifiers

PMCID

1715268

1 reference

7 August 2017

1 reference