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Human Heredity
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March 17, 1999
Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis families
O 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 population
O 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 symptoms
O Loumi, H Cuppens, R Bakour, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
Human Heredity
|
March 17, 1999
Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis families
O 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 population
O 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 symptoms
O Loumi, H Cuppens, R Bakour, et al.
Page
of 1