Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene

By Shalitin S.   Josefsberg Z.   Vilain E.   Shomrat R.   Weintrob N.  

Molecular Genetics and Metabolism, Vol. 76, Iss. 2, 2002-06 ,pp. : 157-161

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Linkage Studies of SOX13, the ICA12 Autoantigen Gene, in Families with Type 1 Diabetes

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Molecular Genetics and Metabolism, Vol. 72, Iss. 4, 2001-04 ,pp. : 356-359

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Significance of Linkage Disequilibrium between Mutation C282Y and a MseI Polymorphism in Population Screening and DNA Diagnosis of Hemochromatosis

By de Villiers J.N.P.   Beutler M.E.J.  

Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 4, 1999-08 ,pp. : 250-252

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Commentary on Significance of Linkage Disequilibrium between Mutation C282Y and a MseI Polymorphism in Population Screening and DNA Diagnosis of Hemochromatosis by J. Nico P. de Villiers and Maritha J. Kotze

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Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 4, 1999-08 ,pp. : 253-254

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CYBB Mutation Analysis in X-Linked Chronic Granulomatous Disease

By Jirapongsananuruk O.   Niemela J.E.   Malech H.L.   Fleisher T.A.  

Clinical Immunology, Vol. 104, Iss. 1, 2002-07 ,pp. : 73-76

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