(Q35889387)

10 August 2017

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19 (English)

1 reference

10 August 2017

0 references

0 references

1 reference

3

Holmberg C

1 reference

10 August 2017

Kestilä M

1

1 reference

10 August 2017

Männikkö M

2

1 reference

10 August 2017

Gyapay G

4

1 reference

10 August 2017

Weissenbach J

5

1 reference

10 August 2017

Savolainen ER

6

1 reference

10 August 2017

Peltonen L

7

1 reference

10 August 2017

Tryggvason K

8

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 May 1994

1 reference

American Journal of Human Genetics

10 August 2017

1 reference

10 August 2017

54

1 reference

10 August 2017

757-764

1 reference

10 August 2017

5

1 reference

Mutations of Bacteria from Virus Sensitivity to Virus Resistance

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Strategies for multilocus linkage analysis in humans

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Main features of the congenital nephrotic syndrome.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Renal transplantation in small children with congenital nephrotic syndrome of the Finnish type.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Congenital nephrotic syndrome of Finnish type. Study of 75 patients

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Prenatal Diagnosis of Congenital Nephrosis in 23 High-Risk Families

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918269

Loss of anionic sites from the glomerular basement membrane in aminonucleoside nephrosis

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8178817

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital nephrotic syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8178817

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

10 August 2017

1 reference