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Clinical and Experimental Rheumatology
|
June 21, 2008
Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapy
C Rooryck, T Barnetche, C Richez, et al.
European Journal of Dermatology : EJD
|
November 10, 2001
Familial aggregation of vitiligo in the French West Indies (Isle of Martinique)
A M Boisseau-Garsaud, I Saint-Cyr, D Quist, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndrome
A Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Gene
|
May 23, 1998
A new yeast artificial chromosome vector designed for gene transfer into mammalian cells
P J Ripoll, A Cowper, S Salmeron, et al.
Human Genetics
|
October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker
A Hanauer, Y Alembik, B Arveiler, et al.
American Journal of Human Genetics
|
May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome
B Arveiler, G de Saint-Basile, A Fischer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient
J Petre, E Lasseaux, C Ged, et al.
American Journal of Medical Genetics
|
May 1, 1988
Improved DNA markers for efficient analysis of fragile X families
R Heilig, I Oberlé, B Arveiler, et al.
Nucleic Acids Research
|
February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C gene
B Arveiler, C Le Van Kim, Y Colin, et al.
Clinical and Experimental Dermatology
|
February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disorders
F Morice-Picard, O Letertre, E Lasseaux, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 64) with videos related to
Sort By:
Page
of 7
Clinical and Experimental Rheumatology
|
June 21, 2008
Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapy
C Rooryck, T Barnetche, C Richez, et al.
European Journal of Dermatology : EJD
|
November 10, 2001
Familial aggregation of vitiligo in the French West Indies (Isle of Martinique)
A M Boisseau-Garsaud, I Saint-Cyr, D Quist, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndrome
A Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Gene
|
May 23, 1998
A new yeast artificial chromosome vector designed for gene transfer into mammalian cells
P J Ripoll, A Cowper, S Salmeron, et al.
Human Genetics
|
October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker
A Hanauer, Y Alembik, B Arveiler, et al.
American Journal of Human Genetics
|
May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome
B Arveiler, G de Saint-Basile, A Fischer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient
J Petre, E Lasseaux, C Ged, et al.
American Journal of Medical Genetics
|
May 1, 1988
Improved DNA markers for efficient analysis of fragile X families
R Heilig, I Oberlé, B Arveiler, et al.
Nucleic Acids Research
|
February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C gene
B Arveiler, C Le Van Kim, Y Colin, et al.
Clinical and Experimental Dermatology
|
February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disorders
F Morice-Picard, O Letertre, E Lasseaux, et al.
Page
of 7