Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Tissue Antigens|December 22, 1999
Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populationsF Clot, M C Fulchignoni-Lataud, C Renoux, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutationsM Medlej-Hashim, I Petit, S Adib, et al.
Human Mutation|March 27, 1999
Characterization of eleven novel mutations (M45L, R119H, 544delG, G145V, H154Y, C184Y, D289V, 862+5A, 1172delC, R411X, E459K) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with severe hypophosphatasia. Mutations in brief no. 217. OnlineA Taillandier, L Zurutuza, F Muller, et al.
Human Genetics|August 2, 2001
A molecular approach to dominance in hypophosphatasiaA S Lia-Baldini, F Muller, A Taillandier, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasiaE Mornet, A Taillandier, S Peyramaure, et al.
Human Mutation|June 20, 2003
Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL geneM Spentchian, Y Merrien, M Herasse, et al.
Human Mutation|July 5, 2001
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasiaA Taillandier, A S Lia-Baldini, M Mouchard, et al.
Annals of Human Genetics|June 21, 2001
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease familiesL Greco, M C Babron, G R Corazza, et al.
Human Mutation|February 19, 2000
Fifteen new mutations (-195C>T, L-12X, 298-2A>G, T117N, A159T, R229S, 997+2T>A, E274X, A331T, H364R, D389G, 1256delC, R433H, N461I, C472S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with hypophosphatasiaA Taillandier, E Cozien, F Muller, et al.
Pageof 5