Hande Çağlayan, Ph. D. , Professor

+90 (212) 359-6881
hande@boun.edu.tr

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Research: Human Molecular Genetics, Human Molecular Evolution

Molecular pathology of heritable bleeding disorders and development of methods for their molecular diagnosis. Identification of FVIII and FIX genes in Turkish patients and the use of these genes as model systems to answer some of the basic concepts in molecular genetics.

Molecular Genetics of Idiopathic Generalized Epilepsy; Molecular pathology of BFNC and EPM1 Epilepsy subtypes in Turkish patients.

Establishment of national mutation databases for hemophilia A and hemophilia B.

Molecular Genetics of Idiopathic Generalized Epilepsy; Molecular pathology of BFNC and EPM1 Epilepsy subtypes in Turkish patients.

Establishment of national mutation databases for hemophilia A and hemophilia B.

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