12 results on '"Oltra S"'
Search Results
2. Epigenetic alterations in disseminated neuroblastoma tumour cells: influence of TMS1 gene hypermethylation in relapse risk in NB patients
3. Subtelomeric analysis of pediatric astrocytoma: Subchromosomal instability is a distinctive feature of pleomorphic xanthoastrocytoma
4. Autosomal-dominant hypohidrotic ectodermal dysplasia caused by a novel mutation
5. Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes
6. Duplication of the Williams–Beuren critical region: case report and further delineation of the phenotypic spectrum
7. Clinical findings and molecular characterization of six subtelomeric imbalances
8. Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II
9. Mutation Profile of the MYO7A Gene in Spanish Patients With Usher Syndrome Type I
10. Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability
11. Early chimerism status predicts engraftment after unrelated-donor umbilical cord blood transplantation
12. Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin–Lowry syndrome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.