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9. Abstract

14. A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: evidence of a founder effect

15. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Barrter syndrome, evidence for genetic heterogeneity

19. Molekulargewichtsbestimmung

26. OOMMF MODELLING OF MAGNETIZATION DYNAMICS IN MICROMETER SIZED STRUCTURES FOR SENSING APPLICATIONS.

27. Untersuchung von speziellen Hemmnissen im Zusammenhang mit der Umweltbewertung in der Planung und Genehmigung der Windenergienutzung an Land und Erarbeitung von Lösungsansätzen : Anlagenband ; Forschungskennzahl 3710 97 119, UBA-FB 001984

28. Untersuchung von speziellen Hemmnissen im Zusammenhang mit der Umweltbewertung in der Planung und Genehmigung der Windenergienutzung an Land und Erarbeitung von Lösungsansätzen : Schlussbericht ; Forschungskennzahl 3710 97 119, UBA-FB 001984

30. Infrared analysis of urinary calculi by a single reflection accessory and a neural network interpretation algorithm

31. Growth and survival of low birthweight infants from 0 to 9 years in a rural area of Ghana. Comparison of moderately low (1501-2000 g) and very low birthweight(1000-1500 g) infants and a local reference population

33. Predictive value of cord blood hematological indices and hemoglobin Barts for the detection of heterozygous alpha-thalassemia-2 in an African-Caribbean population

34. Analytical aspects of the automated CKMB1,2 and CKMM1,2,3 isoform determination and its relation to other biochemical markers

35. Lipids, apolipoprotein-E genotypes and other risk factors of patients with coronary artery disease in Curacao

36. Lipids, apolipoprotein-E genotypes and other risk factors of patients with coronary artery disease in Curaçao

41. ARTIFICIAL NEURAL-NETWORK PREDICTIONS OF URINARY CALCULUS COMPOSITIONS ANALYZED WITH INFRARED-SPECTROSCOPY

43. PARTIAL LEAST-SQUARES REGRESSION FOR ROUTINE ANALYSIS OF URINARY CALCULUS COMPOSITION WITH FOURIER-TRANSFORM INFRARED-ANALYSIS

45. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

46. Nucleation in super-saturated products

50. Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31

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