(Q24539611)

2

0 references

H Shalev

3

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V C Sheffield

4

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D Landau

American Journal of Human Genetics

5

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language of work or name

English

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publication date

November 1998

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published in

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volume

63

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issue

5

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page(s)

1404-10

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cites work

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A simple salting out procedure for extracting DNA from human nucleated cells

24 March 2017

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A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

24 March 2017

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Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity

24 March 2017

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

24 March 2017

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Hereditary renal dysplasia and blindness

7 April 2017

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Genetic identification of two major modifier loci of polycystic kidney disease progression in pcy mice

27 September 2017

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Gene assignment, expression, and homology of human tropomodulin

27 September 2017

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A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

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27 September 2017

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The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling.

27 September 2017

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27 September 2017

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Experience with chronic peritoneal dialysis in infants

27 September 2017

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The Drosophila sloppy paired locus encodes two proteins involved in segmentation that show homology to mammalian transcription factors

30 May 2018

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30 May 2018

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Polycystic kidneys in newborns, infants and children. A clinical and pathological study

30 May 2018

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The effect of paclitaxel on the progression of polycystic kidney disease in rodents.

29 November 2018

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A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p

29 November 2018

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Familial Renal-Retinal Dystrophy

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Medullary Cystic Disease and Familial Juvenile Nephronophthisis

29 November 2018

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12 December 2020

Prevalence, pathogenesis, and functional significance of aldosterone deficiency in hyperkalemic patients with chronic renal insufficiency

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12 December 2020

Programs for pedigree analysis: Mendel, Fisher, and dGene

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12 December 2020

Autosomal recessive polycystic kidney disease

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12 December 2020

Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?

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12 December 2020

Fast and sensitive silver staining of DNA in polyacrylamide gels

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12 December 2020

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

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12 December 2020

Murine autosomal recessive polycystic kidney disease with multiorgan involvement induced by the cpk gene

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12 December 2020

Murine models of polycystic kidney disease

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12 December 2020

Identifiers

DOI

10.1086/302108

1 reference

4101558

4101558

1 reference

1 reference

1 reference