12 results on '"Casals T"'
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2. Common CFTR Haplotypes and Susceptibility to Chronic Pancreatitis and Congenital Bilateral Absence of the Vas Deferens (vol 32, pg 912, 2011)
3. Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis‐like phenotypes
4. CFTR mutations in cystic fibrosis patients from Murcia region (southeastern Spain): implications for genetic testing
5. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles
6. Spectrum of Mutations in the CFTR Gene in Cystic Fibrosis Patients of Spanish Ancestry
7. Molecular evaluation of CFTR sequence variants in male infertility of testicular origin
8. Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations?
9. Prenatal diagnosis of cystic fibrosis by simultaneous analysis of two different mutations
10. Δ F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families
11. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
12. Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families.
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