Abnormal mitochondria in retinoblastoma.

Abnormal hepatocellular mitochondria in methylmalonic acidemia.

Myopathies with abnormal mitochondria: a clinicopathologic classification.

Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study.

Familial progressive external ophthalmoplegia with abnormal muscle mitochondria.

Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome).

Fraternal concordance of types of abnormal hepatocellular mitochondria in Wilson's disease.

Retinoblastoma in transgenic mice.

- mice share abnormal mitochondria.

Loss of Drosophila i-AAA protease, dYME1L, causes abnormal mitochondria and apoptotic degeneration.

Point mutations in retinoblastoma.

Genetic counseling in retinoblastoma.

Retinoblastoma in older children.

Cystic retinoblastoma.

Neonatal Retinoblastoma.

Bilateral retinoblastoma.

Animal models in retinoblastoma research.

Cobalt60 plaques in recurrent retinoblastoma.

Spontaneous mutation rate in retinoblastoma.

Management of Retinoblastoma in Zambia.

Retinoblastoma in Bloch-Sulzberger syndrome.

[Risk of metastasis in retinoblastoma].

Effect of acteoside on the re-localization and abnormal morphology of mitochondria in porcine oocytes during in vitro maturation.

Chemotherapy in Retinoblastoma: Current Approaches.

Associated congenital malformations in retinoblastoma.

Suggest Documents

Abnormal hepatocellular mitochondria in methylmalonic acidemia.

Myopathies with abnormal mitochondria: a clinicopathologic classification.

Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study.

Familial progressive external ophthalmoplegia with abnormal muscle mitochondria.

Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome).

Fraternal concordance of types of abnormal hepatocellular mitochondria in Wilson's disease.

Retinoblastoma in transgenic mice.

- mice share abnormal mitochondria.

Loss of Drosophila i-AAA protease, dYME1L, causes abnormal mitochondria and apoptotic degeneration.

Point mutations in retinoblastoma.

Genetic counseling in retinoblastoma.

Retinoblastoma in older children.

Cystic retinoblastoma.

Neonatal Retinoblastoma.

Bilateral retinoblastoma.

Animal models in retinoblastoma research.

Cobalt60 plaques in recurrent retinoblastoma.

Spontaneous mutation rate in retinoblastoma.

Management of Retinoblastoma in Zambia.

Retinoblastoma in Bloch-Sulzberger syndrome.

[Risk of metastasis in retinoblastoma].

Effect of acteoside on the re-localization and abnormal morphology of mitochondria in porcine oocytes during in vitro maturation.

Chemotherapy in Retinoblastoma: Current Approaches.

Associated congenital malformations in retinoblastoma.

Abnormal mitochondria in retinoblastoma.

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