X chromosome inactivation and the diagnosis of X linked disease in females.

Author:

Brown R M,Brown G K

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. "Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis;Brown, G.K.; Haan, E.A.; Kirby, D.M.;Eur J Pediatr,1988

2. Isolated and combined deficiencies of the a-ketoacid dehydrogenase complexes;Robinson, B.H.; Chun, K.; MacKay, N.;Ann NY Acad Sci,1989

3. Genetic defects in human pyruvate dehydrogenase;Ho, L.; Wexler, I.D.; Kerr, D.S.; Patel, M.S.;Ann NY Acad Sci,1989

4. The clinical and biochemical spectrum of human pyruvate dehydrogenase deficiency;Brown, G.K.; Brown, R.M.; Scholem, R.D.; Kirby, D.M.; Dahl, H.H.M.;Ann NY Acad Sci,1989

5. Molecular biology and biochemistry of pyruvate dehydrogenase complexes;Patel, M.S.; Roche, T.E.;FA SEB J,1990

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