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Results of search for 'au:"Jouanolle, A M"', page 1 of 3
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Authors
Blayau, M
Brissot, P
Chauvel, B
David, V
Deugnier, Y
Dorval, I
Fergelot, P
Gandon, G
Gicquel, I
Guyader, D
Jouanolle, A M
Jouanolle, A-M
Le Gall, J Y
Le Treut, A
Mauvieux, V
Moirand, R
Perichon, M
Pontarotti, P
Yaouanq, J
el Kahloun, A
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Topics
Adult
Aged
Alleles
Chromosomes, Human, Pair 6
Female
Gene Frequency
Genes, MHC Class I
HLA Antigens
Hemochromatosis
Hemochromatosis Protein
Histocompatibility Antigens Class I
Humans
Iron Overload
Male
Membrane Proteins
Middle Aged
Mutation
diagnosis
genetics
metabolism
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Languages
English
French
Your search returned 46 results.
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1.
[Genetic hemochromatosis].
[electronic resource]
by
Jouanolle, A M
David, V
Le Gall, J Y
Producer:
19970821
In:
Annales de biologie clinique
vol. 55
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2.
A highly informative dinucleotide repeat polymorphism telomeric to HLA-F.
[electronic resource]
by
Andrieux, N
Jouanolle, A M
Gandon, G
Mosser, J
Producer:
19970904
In:
Immunogenetics
vol. 46
Online resources:
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3.
Alpha-L-fucosidase in rat testis during sexual maturity.
[electronic resource]
by
Leray, G
Shacoori, V
Prodhomme, C
Jouanolle, A M
Blayau, M
Producer:
19881221
In:
Archives of andrology
vol. 21
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4.
[Iron overload and HFE gene].
[electronic resource]
by
Deugnier, Y
Moirand, R
Guyader, D
Jouanolle, A M
Brissot, P
Producer:
19990517
In:
Gastroenterologie clinique et biologique
vol. 23
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5.
Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.
[electronic resource]
by
Pinson, S
Yaouanq, J
Jouanolle, A M
Turlin, B
Plauchu, H
Producer:
19990204
In:
Journal of medical genetics
vol. 35
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6.
Haemochromatosis Cys282Tyr mutation in pyridoxine-responsive sideroblastic anaemia.
[electronic resource]
by
Yaouanq, J
Grosbois, B
Jouanolle, A M
Goasguen, J
Leblay, R
Producer:
19970612
In:
Lancet (London, England)
vol. 349
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7.
[Genetic hemochromatosis].
[electronic resource]
by
Jouanolle, A M
Gandon, G
Le Gall, J Y
David, V
Producer:
19981207
In:
Annales de biologie clinique
vol. 56 Spec No
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8.
[Comparison of 2 methods of measuring microalbuminuria. Immunonephelometry and radioimmunology].
[electronic resource]
by
Dezier, J F
Jouanolle, A M
Le Reun, M
Poirier, J Y
Producer:
19870616
In:
Annales de biologie clinique
vol. 45
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9.
[Diagnosis of hepatic iron overload].
[electronic resource]
by
Deugnier, Y
Bardou-Jacquet, E
Lainé, F
Gandon, Y
Jouanolle, A-M
Producer:
20120928
In:
La Revue de medecine interne
vol. 33 Suppl 1
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10.
[The diagnosis of hemochromatosis in the era of the gene].
[electronic resource]
by
Brissot, P
Moirand, R
Guyader, D
Jouanolle, A M
David, V
Deugnier, Y
Producer:
19991123
In:
Annales d'endocrinologie
vol. 60
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11.
A novel coding sequence belonging to a new multicopy gene family mapping within the human MHC class I region.
[electronic resource]
by
Vernet, C
Ribouchon, M T
Chimini, G
Jouanolle, A M
Sidibé, I
Pontarotti, P
Producer:
19930430
In:
Immunogenetics
vol. 38
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12.
HFE mutations in insulin resistance-associated hepatic iron overload.
[electronic resource]
by
Guillygomarc'h, A
Mendler, M H
Moirand, R
Jouanolle, A M
David, V
Deugnier, Y
Producer:
20010222
In:
Journal of hepatology
vol. 33
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13.
Geography of HFE C282Y and H63D mutations.
[electronic resource]
by
Merryweather-Clarke, A T
Pointon, J J
Jouanolle, A M
Rochette, J
Robson, K J
Producer:
20001207
In:
Genetic testing
vol. 4
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14.
Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives.
[electronic resource]
by
Moirand, R
Jouanolle, A M
Brissot, P
Le Gall, J Y
David, V
Deugnier, Y
Producer:
19990218
In:
Gastroenterology
vol. 116
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15.
[Molecular genetics of hemochromatosis].
[electronic resource]
by
David, V
Jouanolle, A M
Fergelot, P
Brissot, P
Deugnier, Y
Le Gall, J Y
Producer:
19991123
In:
Annales d'endocrinologie
vol. 60
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16.
Pathophysiological variations in the rat liver plasma membrane serine proteinase activity.
[electronic resource]
by
Guenet, L
Gueble-Val, F
Prodhomme, C
Leray, G
Jouanolle, A M
Le Treut, A
Producer:
19900308
In:
Enzyme
vol. 42
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17.
[Laser immunonephelometry. A new method of determination of microalbuminuria].
[electronic resource]
by
Dezier, J F
Le Reun, M
Le Guerrier, A M
Baudouard, C
Jouanolle, A M
Producer:
19860428
In:
Presse medicale (Paris, France : 1983)
vol. 15
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18.
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
[electronic resource]
by
Jouanolle, A M
Fergelot, P
Gandon, G
Yaouanq, J
Le Gall, J Y
David, V
Producer:
19971119
In:
Human genetics
vol. 100
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19.
Dinucleotide repeat polymorphism at the D6S510 locus.
[electronic resource]
by
Gandon, G
Lelaure, V
Pichon, L
Jouanolle, A M
Le Gall, J Y
David, V
Producer:
19950105
In:
Human molecular genetics
vol. 3
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20.
Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6.
[electronic resource]
by
Mauvieux, V
Jouanolle, A M
el Kahloun, A
Blayau, M
Le Gall, J Y
David, V
Producer:
19920211
In:
Nucleic acids research
vol. 19
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