Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("DELEPINE, Marc")

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 8 of 8

  • Page / 1
Export

Selection :

  • and

Wolcott-rallison syndrome: Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneitySENEE, Valérie; VATTEM, Krishna M; MICHAUD, Jacques L et al.Diabetes (New York, NY). 2004, Vol 53, Num 7, pp 1876-1883, issn 0012-1797, 8 p.Article

Prevalence of mutations in AGPAT2 among human lipodystrophiesMAGRE, Jocelyne; DELEPINE, Marc; SEEMANOVA, Eva et al.Diabetes (New York, NY). 2003, Vol 52, Num 6, pp 1573-1578, issn 0012-1797, 6 p.Article

Fibrinogen and coronary heart disease : test of causality by 'Mendelian randomization'KEAVNEY, Bernard; DANESH, John; PARISH, Sarah et al.International journal of epidemiology. 2006, Vol 35, Num 4, pp 935-947, issn 0300-5771, 13 p.Article

Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk : Genetic epidemiologyKEAVNEY, Bernard; PALMER, Alison; COLLINS, Rory et al.International journal of epidemiology. 2004, Vol 33, Num 5, pp 1002-1013, issn 0300-5771, 12 p.Article

Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital LipodystrophyKIM, C. A; DELEPINE, Marc; SEMPLE, Robert K et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 4, pp 1129-1134, issn 0021-972X, 6 p.Article

Lung cancer susceptibility locus at 5p15.33MCKAY, James D; HUNG, Rayjean J; RUDNAI, Peter et al.Nature genetics. 2008, Vol 40, Num 12, pp 1404-1406, issn 1061-4036, 3 p.Article

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in LebanonZALLOUA, Pierre A; AZAR, Sami T; JULIER, Cécile et al.Human molecular genetics (Print). 2008, Vol 17, Num 24, pp 4012-4021, issn 0964-6906, 10 p.Article

Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndromeKAISAKI, Pamela J; DELEPINE, Marc; SCHURMANS, Stéphane et al.Diabetes (New York, NY). 2004, Vol 53, Num 7, pp 1900-1904, issn 0012-1797, 5 p.Article

  • Page / 1