Resultats de la cerca - Jacques Loiselet
- Mostrar 1 - 8 resultats de 8
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X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3 per André Mégarbané, Nabiha Salem, Edouard Stéphan, Ramzi Ashoush, Didier Lenoir, Valérie Delague, Roland Kassab, Jacques Loiselet, Patrice Bouvagnet
Publicat 2000Artigo -
3
Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate... per Valérie Delague, Corinne Bareil, Sylvie Tuffery‐Giraud, Patrice Bouvagnet, Éliane Chouery, Salam Koussa, Thierry Maisonobe, Jacques Loiselet, André Mégarbané, Mireille Claustres
Publicat 2000Artigo -
4
Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD per Brian C. Verrelli, John H. McDonald, George Argyropoulos, Giovanni Destro‐Bisol, Alain Froment, Anthi Drousiotou, Marie‐Paule Lefranc, Ahmed Noureddine Helal, Jacques Loiselet, Sarah A. Tishkoff
Publicat 2002Artigo -
5
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive... per Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, Elisabeth Verpy, Richard J. Goodyear, Xue Zhong Liu, Sylvie Nouaille, Walter E. Nance, Moien Kanaan, Karen B. Avraham, Fredj Tekaia, Jacques Loiselet, M Lathrop, Guy P. Richardson, Christine Petit
Publicat 2002Artigo -
6
Erratum: Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkBa/NF-kB pathway in limb-girdle muscular dystrophy type 2A per Stephen Baghdiguian, Marianne Martin, Isabelle Richard, F. Pons, C. Astier, Nathalie Bourg, Ronald T. Hay, Roy F. Chemaly, G Halaby, Jacques Loiselet, Louise V.B. Anderson, Adolfo López de Munaín, Michel Fardeau, P. Mangeat, J. Beckmann, Marie‐Paule Lefranc
Publicat 1999Errata/Corrigenda -
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Haplotype Diversity and Linkage Disequilibrium at Human <i>G6PD</i> : Recent Origin of Alleles That Confer Malarial Resistance per Sarah A. Tishkoff, Robert Varkonyi, Nelie Cahinhinan, Salem Abbès, George Argyropoulos, Giovanni Destro‐Bisol, Anthi Drousiotou, Bruce Dangerfield, Marie‐Paule Lefranc, Jacques Loiselet, Anna Piro, Mark Stoneking, Antonio Tagarelli, Giuseppe Tagarelli, Elias H Touma, Scott M. Williams, Andrew G. Clark
Publicat 2001Artigo -
8
Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene per Françoise Denoyelle, Dominique Weil, Marion A. Maw, S.A. Wilcox, Nicholas Lench, D. R. Allen-Powell, Amelia H. Osborn, H Dahl, Anna Middleton, Mark Houseman, Catherine Dodé, Sandrine Marlin, Amel Boulila‐Elgaied, M’hamed Grati, Hammadi Ayadi, S. Benarab, Pierre Bitoun, Geneviève Lina‐Granade, Jacqueline Godet, Mirna Mustapha, Jacques Loiselet, Elie El‐Zir, Anne Aubois, A Joannard, Jacqueline Levilliers, E.N. Garabédian, R F Mueller, R. J McKinlay Gardner, Christine Petit
Publicat 1997Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Medicine
Allele
Locus (genetics)
Phenotype
Anatomy
Cell biology
Computer science
Evolutionary biology
Genetic linkage
Haplotype
Internal medicine
Mutation
Population
Allele frequency
Apoptosis
Artificial intelligence
Atrophy
Biochemistry
Calpain
Chemistry
Chromosomal region
Chromosome
Cochlea
Computational biology
Connexin
Consanguinity
Demography