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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Etienne Mornet

Laboratoire SESEP

Centre Hospitalier de Versailles

Bâtiment EFS

2 rue Jean-Louis Forain

France

[email]@*.uvsq.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Laboratoire SESEP, Centre Hospitalier de Versailles, Bâtiment EFS, 2 rue Jean-Louis Forain, France. 2007 - 2008
  • Laboratoire de Cytogénétique et Génétique Moléculaire Humaine, Université de Versailles-Saint Quentin, France. 1997 - 2000
  • Centre d'Etudes de Biologie Prénatale-SESEP, Université de Versailles, France. 1998 - 2000

References

  1. Hypophosphatasia. Mornet, E. Best. Pract. Res. Clin. Rheumatol (2008) [Pubmed]
  2. Hypophosphatasia. Mornet, E. Orphanet. J. Rare. Dis (2007) [Pubmed]
  3. Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase gene. Mornet, E. Hum. Mutat. (2000) [Pubmed]
  4. A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutations. Mornet, E., Gibrat, J.F. Hum. Genet. (2000) [Pubmed]
  5. Correlation of alkaline phosphatase (ALP) determination and analysis of the tissue non-specific ALP gene in prenatal diagnosis of severe hypophosphatasia. Mornet, E., Muller, F., Ngo, S., Taillandier, A., Simon-Bouy, B., Maire, I., Oury, J.F. Prenat. Diagn. (1999) [Pubmed]
  6. The intermediate alleles of the fragile X CGG repeat in patients with mental retardation. Mornet, E., Chateau, C., Simon-Bouy, B., Serre, J.L. Clin. Genet. (1998) [Pubmed]
  7. Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia. Mornet, E., Taillandier, A., Peyramaure, S., Kaper, F., Muller, F., Brenner, R., Bussière, P., Freisinger, P., Godard, J., Le Merrer, M., Oury, J.F., Plauchu, H., Puddu, R., Rival, J.M., Superti-Furga, A., Touraine, R.L., Serre, J.L., Simon-Bouy, B. Eur. J. Hum. Genet. (1998) [Pubmed]
  8. Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects. Mornet, E., Muller, F., Lenvoisé-Furet, A., Delezoide, A.L., Col, J.Y., Simon-Bouy, B., Serre, J.L. Hum. Genet. (1997) [Pubmed]
 
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