Application of Multiplex ARMS and SSCP/HD Analysis in Molecular Diagnosis of Cystic Fibrosis in Indian Patients

Author:

Ashavaid Tester F.,Kondkar Altaf A.,Dherai Alpa J.,Raghavan Rani,Udani Soonu V.,Udwadia Zarir F.,Desai Devendra

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Reference20 articles.

1. Sarsfield JK, Daves JM. Negative sweat tests and cystic fibrosis: archives of disease in childhood. Arch Dis Child 1975; 50: 463–6

2. Rosenstein BJ. What is a cystic fibrosis diagnosis? In: Fiel SB, editor. Clinics in chest medicine. Philadelphia (PA): Saunders, 1998: 423–41

3. Farrell PM, Koscik RE. Sweat chloride concentrations in infants homozygous and heterozygous for F508 cystic fibrosis. Pediatrics 1996; 97: 524–8

4. Mickle JE, Cutting GR. Clinical implications of cystic fibrosis transmembrane conductance regulator mutations. In: Fiel SB, editor. Clinics in chest medicine. Philadelphia (PA): Saunders, 1998: 443–58

5. Kabra M, Wallace A, Ghosh M, et al. Cystic fibrosis in India: report of 30 cases and frequency of AF508 mutation. Ind J Hum Genet 1998; 4: 103–5

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