Forskning
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Region Hovedstaden - en del af Københavns Universitetshospital
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Expertise

clinical genetics; congenital syndromes and chromosomal disorders including fragile X syndrome and Rett syndrome; molecular genetics of inherited eye disorders; cytogenetics; imprinting disorders; prenatal diagnosis

Primære forskningsområder

Genetics of mental retardation and visual impairment

Aktuel forskning

Investigation of premutation carriers in fragile X syndrome;

Molecular genetic analyses of patients with retinal dystrophy

 

Mulige interessekonflikter

None

ID: 36882327