M Warburg

Deletion mapping of a retinal cone‐rod dystrophy: Assignment to 18q211

M Warburg, O. Sjö, Lisbeth Tranebjærg et al. · American Journal of Medical Genetics · 1991 · 68 citations

Life Sciences, Genetics, Molecular Genetics +14

Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene

Lisbeth Tranebjærg, P. K. A. Jensen, Marijke Van Ghelue et al. · Ophthalmic Genetics · 2001 · 55 citations

Life Sciences, Genetics, Neurology +16

Cytogenetic findings indicate heterogeneity in patients with blepharophimosis, epicanthus inversus, and developmental delay.

M Warburg, M. Bugge, Karen Brøndum‐Nielsen · Journal of Medical Genetics · 1995 · 41 citations · Full text

Life Sciences, Genetics, Pediatrics +17

Interstitial deletion 13q. Further delineation of the syndrome by clinical and high‐resolution chromosome analysis of five patients

Lisbeth Tranebjærg, Karen Brøndum Nielsen, Niels Tommerup et al. · American Journal of Medical Genetics · 1988 · 38 citations

Life Sciences, Genetics, Molecular Genetics +17

The Cohen syndrome:Retinal lesions and granulocytopenia

M Warburg, Søren Anker Pedersen, Henning Hørlyk · Ophthalmic Paediatrics and Genetics · 1990 · 29 citations

Medicine, Neurology, Ophthalmology +8