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1 in total

1. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP.

Authors: X Estivill; C McLean; V Nunes; T Casals; P Gallano; P Scambler; R Williamson
Journal: Am J Hum Genet Date: 1989-05 Impact factor: 11.025

1 in total

11 in total

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

Authors: T Dörk; T Neumann; U Wulbrand; B Wulf; N Kälin; G Maass; M Krawczak; H Guillermit; C Ferec; G Horn
Journal: Hum Genet Date: 1992-02 Impact factor: 4.132

2. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG).

Authors:
Journal: Hum Genet Date: 1990-09 Impact factor: 4.132

3. Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

Authors: J Reiss; D N Cooper; J Bal; R Slomski; G R Cutting; M Krawczak
Journal: Hum Genet Date: 1991-08 Impact factor: 4.132

4. The Irish cystic fibrosis database.

Authors: S M Cashman; A Patino; M G Delgado; L Byrne; B Denham; M De Arce
Journal: J Med Genet Date: 1995-12 Impact factor: 6.318

Review 5. Application of the polymerase chain reaction to the diagnosis of human genetic disease.

Authors: J Reiss; D N Cooper
Journal: Hum Genet Date: 1990-06 Impact factor: 4.132

6. Detection of Epstein-Barr virus in a case of undifferentiated nasopharyngeal carcinoma by in situ hybridization with digoxigenin-labelled PCR-generated probes.

Authors: P Delvenne; B Kaschten; J M Deneufbourg; L Demanez; A Stevenaert; M Reznik; J Boniver
Journal: Virchows Arch A Pathol Anat Histopathol Date: 1993

Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutation.

1. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP.

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

2. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG).

3. Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

4. The Irish cystic fibrosis database.

Review 5. Application of the polymerase chain reaction to the diagnosis of human genetic disease.

6. Detection of Epstein-Barr virus in a case of undifferentiated nasopharyngeal carcinoma by in situ hybridization with digoxigenin-labelled PCR-generated probes.

7. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.

8. Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20.

9. Frequency of delta F508 and haplotype association in Austrian cystic fibrosis families.

10. Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque origin.