(Q35203596)

7 August 2017

X-linked inheritance of Alport syndrome: family P revisited (English)

1 reference

7 August 2017

1 reference

S J Hasstedt

1

1 reference

PubMed ID

6650503

7 August 2017

C L Atkin

series ordinal

2

1 reference

PubMed ID

6650503

7 August 2017

language of work or name

English

0 references

publication date

1 November 1983

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

35

1 reference

7 August 2017

1241-1251

1 reference

7 August 2017

6

1 reference

Partially sex-linked cominant inheritance of interstitial pyelonephritis

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

A general transmission probability model for pedigree data.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Alport's syndrome. A report of 58 cases and a review of the literature

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Alport's syndrome: experience at Hôpital Necker

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Alport's syndrome of hereditary nephritis and deafness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

A simple method of estimating the segregation ratio under complete ascertainment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Segregation Ratios in Alport's Syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Counseling for dominant traits: a correction for the ascertainment bias due to referral for analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Healthy female carriers of a gene for the Alport syndrome: Importance for genetic counseling

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Ascertainment in the sequential sampling of pedigrees

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

Abnormal Segregation in Hereditary Renal Disease with Deafness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685969

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

Chronic hereditary nephritis with nerve deafness. A Nebraska kindred

1 reference

12 December 2020

A follow-up study of hereditary chronic nephritis

1 reference

12 December 2020

A clinical study of hereditary interstitial pyelonephritis

1 reference

12 December 2020

HEREDITARY NEPHRITIS. REPORT OF A KINDRED

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

The genetics of the Alport syndrome

1 reference

12 December 2020

Identifiers

PMCID

1685969

1 reference

7 August 2017

1 reference

PubMed ID

6650503