(Q39129153)

9 September 2017

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel (English)

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9 September 2017

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E Kerem

1

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9 September 2017

Y M Kalman

2

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9 September 2017

Y Yahav

3

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9 September 2017

T Shoshani

4

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9 September 2017

D Abeliovich

5

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9 September 2017

A Szeinberg

6

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9 September 2017

J Rivlin

7

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9 September 2017

H Blau

8

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A Tal

9

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9 September 2017

L Ben-Tur

10

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9 September 2017

1 August 1995

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9 September 2017

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9 September 2017

96

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2

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9 September 2017

193-197

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https://scigraph.springernature.com/pub.10.1007/bf00207378

9 September 2017

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cites work

The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs

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12 December 2020

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

12 December 2020

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

1 reference

12 December 2020

Glycogen storage disease in Israel. A clinical, biochemical and genetic study

1 reference

12 December 2020

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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12 December 2020

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

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12 December 2020

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis.

1 reference

12 December 2020

Worldwide survey of the delta F508 mutation--report from the cystic fibrosis genetic analysis consortium

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12 December 2020

Analysis of biochemical genetic data on Jewish populations: II. Results and interpretations of heterogeneity indices and distance measures with respect to standards

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12 December 2020

Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patients.

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12 December 2020

Cystic fibrosis in Israel: clinical and genetic aspects

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12 December 2020

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

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12 December 2020

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

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12 December 2020

A donor splice mutation (405 + 1 G → A) in cystic fibrosis associated with exon skipping in epithelial CFTR mRNA

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12 December 2020

Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21

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12 December 2020

Ethnic communities in Israel: the genetic blood markers of the Moroccan Jews

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12 December 2020

A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews

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12 December 2020

Identification of the cystic fibrosis gene: genetic analysis

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12 December 2020

High frequency of cystinuria among Jews of Libyan origin

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12 December 2020

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

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12 December 2020

Genetic diseases among Jews

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12 December 2020

A single origin of phenylketonuria in Yemenite Jews

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12 December 2020

Identifiers

DOI

10.1007/BF00207378

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9 September 2017

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