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1. Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

2. SNP association study in PMS2-associated Lynch syndrome

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Books, media, physical & digital resources

3. The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers

4. Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality

5. Corrigendum: Concepts and characteristics of the ‘COST Reference Microplasma Jet’ (2016 J. Phys. D: Appl. Phys. 49 084003)

6. Session 07: Psychology & Counselling 1

8. Lynch Syndrome Caused by Germline PMS2 Mutations:Delineating the Cancer Risk

9. Mutations in ZBTB20 cause Primrose syndrome

10. Contents, Vol. 77, 1997

11. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors

12. Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome

13. Title Page / Table of Contents / Abstracts

14. Contents, Vol. 56, 1991

15. Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma

16. Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma

18. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors

19. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

20. Molecular, Cytogenetic and Linkage Analysis of Chromosome 11p Regions Involved in Wilms’ Tumour and Associated Congenital Diseases

21. Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization

22. Subject Index, Vol. 77, 1997

23. Subject Index Vol. 56, 1991

24. Comparative genomic hybridization analysis of wilms tumors

25. The use of electrostatic interactions to improve the backflushing effect in crossflow microfiltration

29. Concepts and characteristics of the ‘COST Reference Microplasma Jet’.

30. A specific mutation in TBL1XR1 causes Pierpont syndrome.

31. Mutations in ZBTB20 cause Primrose syndrome.

32. Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality.

33. Recurrence and variability of germline EPCAM deletions in Lynch syndrome.

35. Magnetic imaging with femtosecond temporal resolution.

37. Detection of chromosome abnormalities by quantitative fluorescent PCR in ectopic pregnancies.

38. Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma.

39. Comparative genomic hybridization analysis of Wilms tumors.

40. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.

41. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

42. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

43. Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.

44. The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.

45. Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization.