Tuberous sclerosis: possible modification of phenotypic expression by an unlinked dominant gene.

Author:

Rushton A R,Shaywitz B A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis;Borberg, A.;Acta Psychiatrica et Neurologica Scandinavica,1951

2. Tuberous sclerosis: a genetic study;Bundey, S.; Evans, K.;Journal of Neurology, Neurosurgery and Psychiatry,1969

3. Les phacomatoses;Cuendet, J.F.;Bibliotheca Paediatrica,1961

4. Familial occurrence of tuberous sclerosis;Dickerson, W.W.;Archives ofNeurology andPsychiatry,1951

5. Tuberous sclerosis;Donegani, G.; Grattarola, F.R.; Wildi, E.,1972

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1. Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relatives;Clinical Genetics;2008-06-28

2. Lessons from the Eker Rat Model: From Cage to Bedside;Current Molecular Medicine;2004-12-01

3. Tuberous sclerosis. The persistent challenge of clinical diagnosis;Archives of Dermatology;1995-12-01

4. Non-penetrance in tuberous sclerosis.;Journal of Medical Genetics;1991-06-01

5. Recent Linkage Studies in Tuberous Sclerosis.;Annals of the New York Academy of Sciences;1991-04

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