B J Klevering - JoVE Visualize

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The British Journal of Ophthalmology|July 22, 1999

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneB J Klevering, M van Driel, D J van de Pol, et al.

American Journal of Human Genetics|August 26, 2000

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.

Oral Oncology|August 13, 2011

Extra-oral implants: insertion per- or post-ablation?J P J Dings, T J Maal, M S Muradin, et al.

American Journal of Human Genetics|March 26, 1999

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseA Maugeri, M A van Driel, D J van de Pol, et al.

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Showing results (11-20 of 14) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 14 results.

The British Journal of Ophthalmology|July 22, 1999

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneB J Klevering, M van Driel, D J van de Pol, et al.

American Journal of Human Genetics|August 26, 2000

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.

Oral Oncology|August 13, 2011

Extra-oral implants: insertion per- or post-ablation?J P J Dings, T J Maal, M S Muradin, et al.

American Journal of Human Genetics|March 26, 1999

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseA Maugeri, M A van Driel, D J van de Pol, et al.

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