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O Loumi

Showing results (1-10 of 3) with videos related to

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Human Heredity|March 17, 1999
Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis familiesO Loumi, M Baghriche, M Delpech, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 19, 2007
CFTR mutations in the Algerian populationO Loumi, C Ferec, B Mercier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptomsO Loumi, H Cuppens, R Bakour, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Human Heredity|March 17, 1999
Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis familiesO Loumi, M Baghriche, M Delpech, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 19, 2007
CFTR mutations in the Algerian populationO Loumi, C Ferec, B Mercier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptomsO Loumi, H Cuppens, R Bakour, et al.
Pageof 1