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1. Performance of the CMS muon detector and muon reconstruction with proton-proton collisions at root s=13 TeV

2. Detection of Long-Term Instabilities on Altimeter Backscatter Coefficient Thanks to Wind Speed Data Comparisons from Altimeters and Models

3. Impact of Jason-2 Wind Speed Calibration on the Sea State Bias Correction

4. Jason-2 Global Statistical Assessment and Cross-Calibration with Jason-1

5. Overview and Update of the Sea State Bias Corrections for the Jason-2, Jason-1 and TOPEX Missions

6. Benefits of the Future Sea Surface Salinity Measurements From SMOS: Generation and Characteristics of SMOS Geophysical Products

7. Combining Argo and remote-sensing data to estimate the ocean three-dimensional temperature fields—a first approach based on simulated observations

8. [PP.05.32] PROFOUND SYMPATHETIC NERVOUS SYSTEM ACTIVATION IN PATIENTS WTH RESISTANT HYPERTENSION

9. The low-incidence red cell antigen Wra: genetic studies

10. Localization of a locus for Charcot-Marie-Tooth neuropathy type la (CMT1A) to chromosome 17

11. APEX: the Atacama Pathfinder EXperiment

12. Salinity retrieval from SMOS brightness temperatures

13. Impact of SMOS space-time averaging on sea surface salinity retrieval

14. A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I

15. Assignment of the YT blood group locus to chromosome 7q

16. Linkage between the Colton blood group locus and ASSP11 on chromosome 7

17. Assignment of the gene(s) governing Froese and Swann blood group polymorphism to chromosome 17q

18. Assignment of the Waldner blood group locus (WD) to 17q12-q21

19. Secondary metabolites by chemical screening, 26.1 7-O-beta-D-galactosyl-brefeldin A via transglycosylation with Penicillium brefeldianum

20. The Diego blood group locus is located on chromosome 17q

21. A homoallelic Gly317--Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites

22. Etiology and Severity of Pain in Outpatients With HF

23. Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I

24. Genetic linkage between the Kell blood group system and prolactin-inducible protein loci: provisional assignment of KEL to chromosome 7

25. Assignment of the Auberger Red Cell Antigen Polymorphism to the Lutheran Blood Group System: Genetic Justification

26. Contents, Vol. 22, 1978

27. The Colton blood group locus. A linkage analysis

28. The Yt Blood Group System (ISBT No. 011)

29. Genetic linkage data for the Dombrock blood group locus relative to chromosome 1 and chromosome 4 loci

30. The Swann Phenotype 700:4,-41; Genetic Studies

31. Subject Index Vol. 22, 1978

32. Contents, Vol. 39, 1989

33. Population study of electrophoretic polymorphisms of red cell enzymes and plasma proteins in Caucasian Canadians

34. The position of the Radin blood group locus in relation to other chromosome 1 loci

35. Some Blood Group Frequencies in a Caucasian Population

36. No Support for Sex-Esterase D Phenotype Association

37. Infantile hypophosphatasia—Linkage with the RH locus

38. Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter: F13A:HLA:GL01:cen gene order

40. Evidence for genetic linkage between the KEL and YT blood group loci

41. Blood groups in Newfoundlanders

42. Multiplicity of genetic polymorphisms of blood in the Schmiedeleut Hutterites

43. The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man

44. An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa

45. The Yt blood group system (ISBT No. 011). Genetic studies

46. Analysis of linkage relationships of Co, Jk and K with each other and with chromosome 2 loci ACP1 and Km

47. Preliminary serological studies on 31 samples of monoclonal antibodies directed against red cell glycophorins

50. Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter:F13A:HLA:GLO1:cen gene order

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