logo-large
  • Browse Categories

Publications by authors named "Dominique Couet"

Claim this Profile
A
Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
Rania Naoufal, Marine Legendre, Dominique Couet, Brigitte Gilbert-Dussardier, Alain Kitzis

Eur J Med Genet· September 2016


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Osteogenesis imperfecta, tricho-dento-osseous syndrome and intellectual disability: a familial case with 17q21.33-q22 (COL1A1 and DLX3) deletion and 7q32.3-q33 duplication resulting from a reciprocal interchromosomal insertion.
Radu Harbuz, Frédéric Bilan, Dominique Couet, Valérie Charraud, Alain Kitzis

Am J Med Genet A· October 2013


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Complete screening of 50 patients with CHARGE syndrome for anomalies in the CHD7 gene using a denaturing high-performance liquid chromatography-based protocol: new guidelines and a proposal for routine diagnosis.
Frédéric Bilan, Marine Legendre, Valérie Charraud, Barbara Manière, Dominique Couet

J Mol Diagn· January 2012


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
© PubHawk
  • About PubHawk
  • Privacy Policy
  • Sitemap
Socials: