(Q33585895)

28 July 2017

title

Correspondence: Alport's syndrome (English)

1 reference

https://api.crossref.org/works/10.1136/JMG.10.4.396

28 July 2017

1 reference

3 March 2023

1 reference

O. Mayo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4774833

3 March 2023

language of work or name

English

0 references

publication date

1 December 1973

1 reference

full work available at URL

28 July 2017

https://europepmc.org/articles/PMC1013066

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4774833

https://europepmc.org/articles/PMC1013066?pdf=render

3 March 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4774833

https://syndication.highwire.org/content/doi/10.1136/jmg.10.4.396

3 March 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.10.4.396

Journal of Medical Genetics

3 March 2023

published in

1 reference

28 July 2017

volume

10

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

396-398

1 reference

Abnormal Segregation in Hereditary Renal Disease with Deafness

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013066

A genetic study of hereditary renal dysfunction with associated nerve deafness

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013066

Segregation Ratios in Alport's Syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013066

Syndrome of hereditary hematuria, nephropathy and deafness.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013066

On the maintenance of polymorphisms having an inviable homozygote

31 October 2018

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

Hereditary nephritis. Early clinical, functional, and morphological studies

1 reference

12 December 2020

HEREDITARY NEPHRITIS. REPORT OF A KINDRED

1 reference

12 December 2020

HEREDITARY RENAL DYSFUNCTION AND DEAFNESS

1 reference

12 December 2020

DIAGNOSTIC VALUE OF SERUM COMPLEMENT DETERMINATION IN HEREDITARY GLOMERULONEPHRITIS

1 reference

12 December 2020

Familial and nonfamilial benign hematuria

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.10.4.396

1 reference

28 July 2017

1 reference

28 July 2017

1 reference