24 results on '"Caballin, M.R."'
Search Results
2. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome
3. Presenting features of 201 children with acute lymphoblastic leukemia: Comparison according to presence or absence of ETV6/RUNX1 rearrangement
4. Prenatal detection of rare chromosomal autosomal abnormalities in Europe
5. P-171. Lack of chromosomal instability in spermatozoa from men affected by testicular cancer
6. ETV6/RUNX1 rearrangement in childhood B-precursor acute lymphoblastic leukemia with normal karyotypes or without cytogenetic results
7. Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes
8. Chromosome inversions involved in the chromosome evolution of the Hominidae and in human constitutional chromosome abnormalities
9. AML1 amplification in a child with acute lymphoblastic leukemia
10. Translocation yields in peripheral blood lymphocytes from control populations.
11. Human sperm chromosomes.
12. Banding Patterns of the Chromosomes of A teles geoffroyi with Description of Two Cases of Pericentric Inversion
13. Growth and Body Proportions in Diabetic Children
14. Cytogenetic study of a patient with the Sézary syndrome
15. Cytogenetic studies in acute nonlymphocytic leukemia
16. Constitutional del(3)(p14–p21) in a patient with bladder carcinoma
17. Chromosome instability in bladder carcinoma patients
18. Cytogenetic findings in three bladder carcinomas
19. Cytogenetic studies in a chromophobe renal cell carcinoma
20. Hereditary renal cell carcinoma of papillary type
21. Cytogenetic studies in a case of familial renal cell carcinoma
22. Isochromosome 14q in myeloid dysplastic disorder
23. Centromere detection in radiation-induced micronuclei of two-cell human-hamster embryos
24. Hamster origin of multiple chromosome rearrangements in first cleavage human-hamster embryos
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