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Your search keyword '"Redon R"' showing total 4 results
Start Over Author "Redon R" Publisher british medical association
4 results on '"Redon R"'

1. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

Author

Jacquemont, M.-L., Sanlaville, D., Redon, R., Raoul, O., Cormier-Daire, V., Lyonnet, S., Amiel, J., Merrer, M. Le, Heron, D., Blois, M.-C. de, Prieur, M., Vekemans, M., Carter, N.P., Munnich, A., Colleaux, L., and Philippe, A.

Subjects
Autism -- Genetic aspects, In situ hybridization -- Usage, In situ hybridization -- Research, Human chromosome abnormalities -- Identification and classification, Human chromosome abnormalities -- Diagnosis, Health
Published
2006

3. Microarray based comparative genomic hybridisation (array-CGH) detects submicrosocopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

Author

Shaw-Smith, C., Redon, R., Rickman. L., Rio, M., Willatt, L., Fiegler, H., Firth, H., Sanlaville, D., Winter, R., Colleaux, L., Bobrow, M., and Carter, N.P.

Subjects
Learning disabilities -- Causes of, Learning disabilities -- Research, Mental retardation -- Causes of, Mental retardation -- Research, Human chromosomes -- Research, Genomics -- Research, Health
Published
2004

4. NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.

Author

Borck G, Redon R, Sanlaville D, Rio M, Prieur M, Lyonnet S, Vekemans M, Carter NP, Munnich A, Colleaux L, and Cormier-Daire V

Subjects
Adolescent, Adult, Cell Cycle Proteins, Child, Child, Preschool, Chromosome Aberrations, Chromosomes, Human, Pair 18, Cytogenetic Analysis, Female, Follow-Up Studies, Humans, Infant, Karyotyping, Male, Parents, De Lange Syndrome genetics, Genetic Heterogeneity, Mutation, Proteins genetics
Published
2004
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