AAAAAA

   
Results: 1-11 |
Results: 11
HEMOCHROMATOSIS AND HLA-H
Authors: JOUANOLLE AM GANDON G JEZEQUEL P BLAYAU M CAMPION ML YAOUANQ J MOSSER J FERGELOT P CHAUVEL B BOURIC P CARN G ANDRIEUX N GICQUEL I LEGALL JY DAVID V
Citation: Am. Jouanolle et al., HEMOCHROMATOSIS AND HLA-H, Nature genetics, 14(3), 1996, pp. 251-252
IDENTIFICATION OF A NOVEL MUTATION (A268G) IN EXON-8 OF THE HTR-BETA GENE IN A LARGE FAMILY WITH THYROID-HORMONE RESISTANCE
Authors: JEZEQUEL P GUILHEM I HESPEL JP LETREUT A LEGALL JY ALLANNIC H BLAYAU M
Citation: P. Jezequel et al., IDENTIFICATION OF A NOVEL MUTATION (A268G) IN EXON-8 OF THE HTR-BETA GENE IN A LARGE FAMILY WITH THYROID-HORMONE RESISTANCE, Human mutation, 8(4), 1996, pp. 396-396
IDENTIFICATION OF A NOVEL MUTATION IN CFTR GENE EXON-8 (L375F) IN A CUAVD PHENOTYPE
Authors: JEZEQUEL P CHAUVEL B LETREUT A LEGALL JY DAVID V LELANNOU D BLAYAU M
Citation: P. Jezequel et al., IDENTIFICATION OF A NOVEL MUTATION IN CFTR GENE EXON-8 (L375F) IN A CUAVD PHENOTYPE, Human genetics, 97(4), 1996, pp. 548-549
FRENCH CF FAMILY GENOTYPE ANALYSIS SHOWS THAT THE R297Q MUTATION IS ARARE POLYMORPHISM
Authors: DORVAL I JEZEQUEL P CHAUVEL B DUBOURG C FERGELOT P LEGALL JY ROUSSEY M BLAYAU M
Citation: I. Dorval et al., FRENCH CF FAMILY GENOTYPE ANALYSIS SHOWS THAT THE R297Q MUTATION IS ARARE POLYMORPHISM, Human mutation, 6(4), 1995, pp. 334-335
OBSTRUCTIVE AZOOSPERMIA WITH AGENESIS OF VAS-DEFERENS OR WITH BRONCHIECTASIA (YOUNGS SYNDROME) - A GENETIC APPROACH
Authors: LELANNOU D JEZEQUEL P BLAYAU M DORVAL I LEMOINE P DABADIE A ROUSSEY M LEMAREC B LEGALL JY
Citation: D. Lelannou et al., OBSTRUCTIVE AZOOSPERMIA WITH AGENESIS OF VAS-DEFERENS OR WITH BRONCHIECTASIA (YOUNGS SYNDROME) - A GENETIC APPROACH, Human reproduction, 10(2), 1995, pp. 338-341
STRUCTURAL-ANALYSIS OF CFTR GENE IN CONGENITAL BILATERAL ABSENCE OF VAS-DEFERENS
Authors: JEZEQUEL P DORVAL I FERGELOT P CHAUVEL B LETREUT A LEGALL JY LELANNOU D BLAYAU M
Citation: P. Jezequel et al., STRUCTURAL-ANALYSIS OF CFTR GENE IN CONGENITAL BILATERAL ABSENCE OF VAS-DEFERENS, Clinical chemistry, 41(6), 1995, pp. 833-835
MOLECULAR-GENETICS OF HEMOCHROMATOSIS
Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, La Semaine des hopitaux de Paris, 70(21-22), 1994, pp. 644-650
ANONYMOUS MARKER LOCI WITHIN 400 KB OF HLA-A GENERATE HAPLOTYPES IN LINKAGE DISEQUILIBRIUM WITH THE HEMOCHROMATOSIS GENE (HFE)
Authors: YAOUANQ J PERICHON M CHORNEY M PONTAROTTI P LETREUT A ELKAHLOUN A MAUVIEUX V BLAYAU M JOUANOLLE AM CHAUVEL B MOIRAND R NOUEL O LEGALL JY FEINGOLD J DAVID V
Citation: J. Yaouanq et al., ANONYMOUS MARKER LOCI WITHIN 400 KB OF HLA-A GENERATE HAPLOTYPES IN LINKAGE DISEQUILIBRIUM WITH THE HEMOCHROMATOSIS GENE (HFE), American journal of human genetics, 54(2), 1994, pp. 252-263
ANALYSIS OF 160-CF CHROMOSOMES - DETECTION OF A NOVEL MUTATION IN EXON-20
Authors: DORVAL I ODENT S JEZEQUEL P JOURNEL H CHAUVEL B DABADIE A ROUSSEY M LEGALL JY LEMAREC B DAVID V BLAYAU M
Citation: I. Dorval et al., ANALYSIS OF 160-CF CHROMOSOMES - DETECTION OF A NOVEL MUTATION IN EXON-20, Human genetics, 91(3), 1993, pp. 254-256
MOLECULAR-GENETICS OF HEMOCHROMATOSIS
Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, Annales de Gastroenterologie et d'Hepatologie, 29(6), 1993, pp. 292-299
MOLECULAR-GENETICS OF HEMOCHROMATOSIS
Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, Bulletin de l'Academie nationale de medecine, 177(2), 1993, pp. 187-201
Risultati: 1-11 |