Survey of CF mutations in the clinical laboratory.

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Detecting Common CFTR Mutations by Reverse Dot Blot Hybridization Method in Cystic Fibrosis First Report from Northern Iran.

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Survey of CF mutations in the clinical laboratory.

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2002 nî lūn-bûn

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2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

Survey of CF mutations in the clinical laboratory

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Survey of CF mutations in the clinical laboratory.

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Survey of CF mutations in the clinical laboratory.

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Survey of CF mutations in the clinical laboratory

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Survey of CF mutations in the clinical laboratory.

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Survey of CF mutations in the clinical laboratory.

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Survey of CF mutations in the clinical laboratory

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Survey of CF mutations in the clinical laboratory

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Survey of CF mutations in the clinical laboratory.

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Survey of CF mutations in the clinical laboratory.

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P1476

Survey of CF mutations in the clinical laboratory.

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P2093

Angela Myers

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Borka Mirkovic

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Klaus Huber

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Kurt Bauer

http://www.w3.org/2001/XMLSchema#string

Randall Saiki

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Rhea Nersesian

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P2860

Identification of the cystic fibrosis gene: chromosome walking and jumping

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

Identification of the cystic fibrosis gene: genetic analysis

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis.

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.

CFTR gene variant IVS8-5T in disseminated bronchiectasis.

Cellular heterogeneity of CFTR expression and function in the lung: implications for gene therapy of cystic fibrosis.

Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease.

Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic Fibrosis.

P2888

1472-6890-2-4

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scholarly article

P356

10.1186/1472-6890-2-4

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2002-11-01T00:00:00Z

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11029786

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P6179

1003919098

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P698

12437773

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P921

Cho͘-chit-ha̍k

P932

138794

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Survey of CF mutations in the clinical laboratory.

about

P2860

P2860

Survey of CF mutations in the clinical laboratory.

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P1433

P1476

P2093

P2860

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P2888

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P356

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P577

P5875

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P698

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P932