207 results on '"Vege, S"'
Search Results
2. P‐IG‐34 | Novel FUT1 Variant c.789C>A in Patient with Para‐Bombay Phenotype and Evaluation by Protein Modeling
3. OA3‐AM23‐TU‐12 | Six Novel RHCE Alleles Identified in Investigation of Donor Antigen Typing Discrepancies
4. P‐IG‐27 | Investigation of Four Patient Samples with Weak D Typing Revealed Four Novel RHD Alleles
5. OA2‐AM23‐TU‐12 | RHD Genotyping for Transfusion of D+ RHD Genotype‐Matched Units to D+ Patients with History of Anti‐D
6. P‐IG‐23 | Identification of a Novel B(972T) Allele in a Blood Donor Associated with B(A) Phenotype
7. P‐IG‐2 | N Antigen Discrepancy Between Serologic and DNA Testing Explained by the Hybrid GYP(B‐A‐B) Allele Encoding the GP.Mur Phenotype
8. “Levine-Critchley syndrome” - obsolete
9. Diagnostic strategy and timing of intervention in infected necrotizing pancreatitis: an international expert survey and case vignette study
10. An RHD*455C Allele Encodes a Partial D Phenotype Associated With Production of Allo Anti-D: SP299
11. New A and B Alleles Associated With Weak Antigen Expression: SP283
12. The Molecular Basis For Jsb Typing Discrepancies In African American Blood Donors: SP282
13. A New High Prevalence Kell Antigen KYOR, Antithetical to the Low-prevalence Antigen KYO, Is the Second Trypsin-sensitive Kell Antigen: SP278
14. A New KEL*230G>T Change Associated With K0 Phenotype In a Patient Presenting With Anti-Kpb: SP277
15. McLeod Phenotypes in Hispanics and Potential Clinical Relevance of XK Genotyping: SP275
16. E Antigen Typing Discrepancy Reveals a Novel 674C>G Change (Ser225Cys) on RhCe Responsible for Expression of Some E Epitopes: S54-030I
17. The Labeling of Antigen Negative Blood and Subsequent Discrepancies: A Retrospective Review: S36-020C
18. RHD Zygosity Testing: SP327
19. Weak D Type 2 and Production of Anti-D: S91-040B
20. Surprising Findings with RBCs Expressing the Low Prevalence RH Antigen Evans: S78-030K
21. RH Haplotypes Among African American Blood Donors: S77-030K
22. A New High Prevalence Antigen (KHUL) in the Kell Blood Group System: S56-030E
23. Two Novel JKA Alleles in a Jk(a+b-) Patient with Anti-Jka: S53-030E
24. Metabolic and target organ outcomes after total pancreatectomy: Mayo Clinic experience and meta-analysis of the literature
25. Universal DNA Arrays for High-Throughput SNP Detection of Human Erythrocyte Antigens (HEA): SP324
26. High Throughput DNA Molecular Testing of African American Donors: An Efficient and Productive Method to Provide Phenotyped Red Cells: SP323
27. Impact of Molecular Testing on Fill Rates in the American Rare Donor Program: SP316
28. A Efficient Screening Method to Detect the Rare RN Haplotype in Blood Donors: SP251
29. RH Alleles Associated with Donor U.S. RhD Typing Discrepancies: SP249
30. Frequency Of RHCE*ce(254G>C) in African-American Patients and Donors: SP235
31. A Pilot Study Using Genotyping to Resolve Donor ABO Discrepancies to Retain Group O Donors: SP232
32. Comparison of Manual and Automated Methods for Diagnosis of Altered RH Alleles: SP245
33. A Screening Method to Find Rare hrB_ Donors by Large-Scale Screening: SP250
34. RHCE*ce(1025C>T) Encodes Partial C and E Antigens: SP239
35. Diversity of RHCE and Identification of Twelve New Alleles: S112-040C
36. New RHD Alleles Associated with Reduced D Antigen Expression: S110-040C
37. Novel Mutations In EKLF/KLF1 Encoding In(Lu) Phenotype: S107-040C
38. KCAM Incidence in a US Midwestern Population: SP185
39. RHD Exon Consensus Splice-Site Changes, 334A>G and 1228T>G, Associated with Weak D Expression: SP172
40. Six New Group A Alleles Associated with ABO Typing Discrepancies: SP156
41. A Case Study of a B Subgroup Patient: Serological Results Supported by Molecular Testing: SP157
42. JK Alleles Associated With Altered Kidd Antigen Expression: S116-040E
43. The Dllla Allele is Linked to Altered Rhce Alleles: S30-020C
44. A Novel 254 G >C (Ala85 Gly) Change Associated with Partial Rhe and Alloanti-e: S32-020C
45. Alloanti-c in a c-positive, JAL-positive patient
46. The RHCE*ceSL Allele Encodes a Weak e Antigen: *SP346
47. The RHCE*ceMO Allele Is Linked to RHD*DAU0 and Encodes an hrS - and hrB - Red Cell Phenotype: *SP339
48. The Weak D Type 2 Mutation 1154G>C Is Associated With Exon Skipping: *SP345
49. A New RHce Allele, RHCE*ceTI, Is Associated with C Typing Discrepancies and Is Linked to RHD*DIVa: *SP342
50. DIIIa and DIII Type 5 partial D Phenotypes Are Encoded by the Same RHD Variant Allele: *SP340
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