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Results of search for 'au:"Ferrec, M"'
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Authors
Bonnefont, J P
Couloigner, V
Djadi-Prat, J
Edelman, A
Elie, C
Ferrec, M
Feuillet-Fieux, M N
Gigarel, N
Guillot, M
Lacour, B
Lenoir, G
Magen, M
Manach, Y
Sermet, I
Steffann, J
Thuillier, L
Torossi, T
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Topics
Adolescent
Adult
Alleles
Black People
Child, Preschool
Codon, Nonsense
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
DNA Mutational Analysis
Exons
Female
Homozygote
Humans
Infant
Infant, Newborn
Loss of Heterozygosity
Male
Mutation
Nasal Polyps
genetics
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English
Your search returned 3 results.
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1.
Novel CFTR mutations in black cystic fibrosis patients.
[electronic resource]
by
Feuillet-Fieux, M N
Ferrec, M
Gigarel, N
Thuillier, L
Sermet, I
Steffann, J
Lenoir, G
Bonnefont, J P
Producer:
20040617
In:
Clinical genetics
vol. 65
Online resources:
Available from publisher's website
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No items available.
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2.
Identification of a novel mutation, 1087delT, in exon 7 of the CFTR gene in a patient with cystic fibrosis.
[electronic resource]
by
Feuillet-Fieux, M N
Sermet, I
Edelman, A
Torossi, T
Ferrec, M
Guillot, M
Lenoir, G
Bonnefont, J P
Thuillier, L
Producer:
20000825
In:
Human mutation
vol. 16
Online resources:
Available from publisher's website
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No items available.
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3.
Nasal polyposis and cystic fibrosis(CF): review of the literature.
[electronic resource]
by
Feuillet-Fieux, M N
Lenoir, G
Sermet, I
Elie, C
Djadi-Prat, J
Ferrec, M
Magen, M
Couloigner, V
Manach, Y
Lacour, B
Bonnefont, J P
Producer:
20111025
In:
Rhinology
vol. 49
Online resources:
Available from publisher's website
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No items available.
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