The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles

By Benayoun Brnice A.   Caburet Sandrine   Dipietromaria Aurlie   Bailly-Bechet Marc   Batista Frank   Fellous Marc   Vaiman Daniel   Veitia Reiner A.  

Human Molecular Genetics, Vol. 17, Iss. 20, 2008-10 ,pp. : 3118-3127

Oxford University Press

Access to resources Recommend Favorite

Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms

By Ramsay Andrew J.   Quesada Victor   Sanchez Mayka   Garabaya Cecilia   Sard Mara P.   Baiget Montserrat   Remacha Angel   Velasco Gloria   Lpez-Otn Carlos  

Human Molecular Genetics, Vol. 18, Iss. 19, 2009-10 ,pp. : 3673-3683

Oxford University Press

Access to resources Recommend Favorite

Prevalence of Three Hereditary Hemochromatosis Mutant Alleles in the Michigan Caucasian Population

By  

Public Health Genomics, Vol. 8, Iss. 3, 2005-08 ,pp. : 173-179

Karger

Access to resources Recommend Favorite

Heterozygosity of mannose-binding lectin ( MBL2 ) genotypes predicts advantage (heterosis) in relation to fatal outcome in intensive care patients

By Hellemann Dorthe   Larsson Anders   Madsen Hans O.   Bonde Jan   Jarlv Jens Otto   Wiis Jrgen   Faber Torsten   Wetterslev Jrn   Garred Peter  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3071-3080

Oxford University Press

Access to resources Recommend Favorite

Structural Analysis of the Minisatellite Present at the 3′ end of the Human Apolipoprotein B Gene: New Definition of the Alleles and Evolutionary Implications

By Buresi Catherine  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 61-68

Oxford University Press

Access to resources Recommend Favorite