A. Taillandier

Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia (2001)

Taillandier, A., Lia-Baldini, A.S., Mouchard, M., Robin, B., Muller, F., Simon-Bouy, B., ...

Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney tissue alkaline phosphatase (L/B/K ALP) activity. We...

Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia (2001)

Taillandier, A., Lia-Baldini, A.S., Mouchard, M., Robin, B., Muller, F., Simon-Bouy, B., ...

Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney tissue alkaline phosphatase (L/B/K ALP) activity. We...

A molecular approach to dominance in hypophosphatasia. (2001)

LIA-BALDINI, AS, MULLER, F, TAILLANDIER, A, GIBRAT, JF, MOUCHARD, M, ROBIN, B, ...

Correlations of genotype and phenotype in hypophosphatasia (1999)

Zurutuza, L, Muller, F, Gibrat, JF, Taillandier, A, Simon-Bouy, B, Serre, JL, ...

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range (1996)

Mornet, E, Chateau, C, Hirst, MC, Thepot, F, Taillandier, A, Cibois, O, ...

Molecular study of three cases of odontohypophosphatasia resulting from heterozygosity for mutations in the tissue non-specific alkaline phosphatase gene

Herasse, M, Spentchian, M, Taillandier, A, Keppler-Noreuil, K, Fliorito, A, Bergoffen, J, ...