(Q24534437)

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Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites

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Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites (English)

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1 reference

S Bolk

1

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E G Puffenberger

series ordinal

2

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J Hudson

series ordinal

3

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D H Morton

series ordinal

4

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A Chakravarti

series ordinal

5

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language of work or name

English

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publication date

December 1999

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published in

American Journal of Human Genetics

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volume

65

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page(s)

1785-90

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issue

6

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cites work

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

1 reference

stated in

PubMed Central

reference URL

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retrieved

24 March 2017

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

retrieved

24 March 2017

Elevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift alone

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

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24 March 2017

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

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24 March 2017

BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

retrieved

27 September 2017

Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

retrieved

27 September 2017

Heredity in the congenital nephrotic syndrome. A genetic study of 57 finnish FAMILIES WITH A REVIEW OF REPORTED CASES

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288392

retrieved

27 September 2017

Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10577936

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adequate clinical control of congenital nephrotic syndrome by enalapril

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10577936

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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ResearchGate publication ID

12723190

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(Q24534437)

Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites

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