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573 results on '"Susan Kupka"'

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1. PGK1 a Potential Marker for Peritoneal Dissemination in Gastric Cancer

2. Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds

3. Mitochondriale A1555G-Mutation

4. Phänotypische Charakterisierung einer DFNA6-Familie mit Tieftonschwerhörigkeit

5. A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by TECTA Mutations

6. Paragangliome der Kopf-Hals-Region

7. Klinische und molekulargenetische Analyse monozygoter Zwillinge mit Stapes-Gusher-Syndrom (DFN3)

8. A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

9. Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness

10. Mutationsanalyse des Connexin26-Gens bei sporadischen Fällen mittel- bis hochgradiger Schwerhörigkeit

11. MSH2 and CXCR4 involvement in malignant VIPoma

12. Human precision-cut liver tumor slices as a tumor patient-individual predictive test system for oncolytic measles vaccine viruses

13. HIES

14. Hereditary Motor and Sensory Neuropathy

15. Hypersulfaturia

16. HLP

17. Uric Acid Nephrolithiasis

18. Bronchopulmonary Dysplasia

19. HSH

20. Hematemesis

21. Urolithiasis, Calcium Oxalate

22. Hyperostosis Corticalis Deformans Juvenilis

23. Human Transmissible Spongiform Encephalopathies

24. Hypercapnia

25. Hereditary Nephritis

26. Branchial Cleft Cyst

27. Hearing Loss, Noise-induced and Acoustic Trauma

28. Hemothorax

29. Brachydactyly

30. Hyperbilirubinemia

31. HRSV

32. Hypersensitivity Type I

33. HCPS

34. Hyperopia

35. Hypoglycemia, Non-islet Cell

36. Hyper-IgE Recurrent Infection Syndrome

37. Hypermobility Syndrome

38. Basal Ganglia Disease, Adult Onset

39. Heat Stroke

40. Hypothyroidism

41. Hyperostose en Coulée

42. Hyperekplexia, Hereditary

43. Hydroxykynureninuria

44. B-Variant of the GM2-Gangliosidoses

45. Hypocalcemia

46. Hand-Heart Syndrome

47. Hypoosmolality

48. Hyperostosis, Infantile Cortical

49. HOA

50. Hypermagnesemia

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