(Q24539127)

12

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Thilo Dörk

object named as

T Dörk

1

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author name string

E H El-Harith

2

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M Stuhrmann

3

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M Macek

4

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M Egan

5

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G R Cutting

6

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E Kanavakis

8

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S Carles

9

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M Claustres

10

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C Padoa

11

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J Schmidtke

American Journal of Human Genetics

13

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language of work or name

English

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publication date

August 1998

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published in

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volume

63

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issue

2

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page(s)

656-62

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cites work

Characterization of nondeletion alpha-thalassemia mutations in the Greek population

1 reference

7 January 2021

Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.

1 reference

7 January 2021

Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphicCFTR DNA markers

1 reference

7 January 2021

Why is the cystic fibrosis gene so frequent?

1 reference

7 January 2021

Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients

1 reference

7 January 2021

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families

1 reference

7 January 2021

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

1 reference

7 January 2021

CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France.

1 reference

7 January 2021

Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival.

1 reference

7 January 2021

Patterns of polymorphism and linkage disequilibrium for cystic fibrosis

1 reference

7 January 2021

Multiplex PCR amplification of three microsatellites within the CFTR gene

1 reference

7 January 2021

Same-day, first-trimester antenatal diagnosis for cystic fibrosis by gene amplification

1 reference

7 January 2021

The origin of the major cystic fibrosis mutation (delta F508) in European populations.

1 reference

7 January 2021

Haplotype analysis to determine the position of a mutation among closely linked DNA markers

1 reference

7 January 2021

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.

1 reference

7 January 2021

CFTR haplotype backgrounds on normal and mutant CFTR genes

1 reference

7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

1 reference

7 January 2021

Cystic Fibrosis Heterozygote Resistance to Cholera Toxin in the Cystic Fibrosis Mouse Model

1 reference

7 January 2021

First report of CFTR mutations in black cystic fibrosis patients of southern African origin

1 reference

7 January 2021

Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis.

1 reference

7 January 2021