(Q39013436)

English

Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population

scientific article published on April 1996

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

congenital disorder

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nephrotic syndrome

1 reference

based on heuristic

inferred from title

author name string

A Fuchshuber

1

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

P Niaudet

2

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

O Gribouval

3

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

G Jean

4

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

M C Gubler

5

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

M Broyer

6

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

C Antignac

7

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

publication date

1 April 1996

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

135-138

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Pax-2 is a DNA-binding protein expressed in embryonic kidney and Wilms tumor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease gene mapping in isolated human populations: the example of Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Faster sequential genetic linkage computations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 1993-94 Généthon human genetic linkage map

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LODVIEW: a computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrotic syndrome of Finnish type. Study of 75 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Finnish population structure A genetic and genealogical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal proteinuria in diagnosis of congenital nephrosis detected by raised alpha-fetoprotein in maternal serum

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703694

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004670050081

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

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