Diagnostic and genetical aspects of tuberous sclerosis.

Author:

Nevin N C,Pearce W G

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases;Blank, C.E.;Ann. hum. Genet,1960

2. Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis: Contribution to elucidation of interrelationship and eugenics of syndromes;Borberg, A.;Acta psychiat. scand,1951

3. Congenital neurocutaneous syndromes in childhood: II Tuberous sclerosis;Chao, D.H.C.;J. Pediat; Infantile spasms and skin anomalies,1959

4. Tuberose sclerosis and allied conditions;Critchley, M.; Earl, C.J.C.;Brain,1932

5. Pulmonary tuberous sclerosis and its relationship to other forms of the disease;Dawson, J.;Quart. J. Med,1954

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