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Results 81 - 90 of 253 for Blood group B
  1. Omenn syndrome 
    ... Citation on PubMed Ege M, Ma Y, Manfras B, Kalwak K, Lu H, Lieber MR, Schwarz K, Pannicke U. Omenn syndrome due to ARTEMIS mutations. Blood. 2005 Jun 1;105(11):4179-86. doi: ...
    https://medlineplus.gov/genetics/condition/omenn-syndrome - Genetics
  2. Barth syndrome 
    ... a substance called 3-methylglutaconic acid in their blood and urine. The amount of the acid does not appear to influence the signs and symptoms of the condition. Barth syndrome is one of a group of metabolic disorders that can be diagnosed by ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  3. CIITA gene 
    ... S, Steimle V, Ucla C, Eibl MM, Mach B. Two novel mutations in the MHC class II transactivator CIITA in a second patient from MHC class II deficiency complementation group A. Hum Genet. 1997 Apr;99(4):541- ...
    https://medlineplus.gov/genetics/gene/ciita - Genetics
  4. VKORC1 gene 
    ... D, Williams MS, Watson MS, Flockhart DA, Gage B, Gandolfi R, King R, Lyon E, Nussbaum R, O'Kane D, Schulman K, Veenstra D, Williams MS, Watson MS; ACMG Working Group on Pharmacogenetic Testing of CYP2C9, VKORC1 Alleles for ...
    https://medlineplus.gov/genetics/gene/vkorc1 - Genetics
  5. Warfarin sensitivity 
    ... D, Williams MS, Watson MS, Flockhart DA, Gage B, Gandolfi R, King R, Lyon E, Nussbaum R, O'Kane D, Schulman K, Veenstra D, Williams MS, Watson MS; ACMG Working Group on Pharmacogenetic Testing of CYP2C9, VKORC1 Alleles for ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
  6. CYP2C9 gene 
    ... D, Williams MS, Watson MS, Flockhart DA, Gage B, Gandolfi R, King R, Lyon E, Nussbaum R, O'Kane D, Schulman K, Veenstra D, Williams MS, Watson MS; ACMG Working Group on Pharmacogenetic Testing of CYP2C9, VKORC1 Alleles for ...
    https://medlineplus.gov/genetics/gene/cyp2c9 - Genetics
  7. TET2 gene 
    ... Vainchenker W, Najman A, Bellanne-Chantelot C; French Group of Familial Myeloproliferative Disorders. Analysis of the ten-eleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms. Blood. 2009 Aug 20;114(8):1628-32. doi: ...
    https://medlineplus.gov/genetics/gene/tet2 - Genetics
  8. Familial hemophagocytic lymphohistiocytosis 
    ... Ehlert K, Gross-Wieltsch U, Jorch N, Kremens B, Pekrun A, Sparber-Sauer M, Mejstrikova E, ... type 5 (FHL5). Blood. 2012 Jun 21;119(25):6016-24. doi: ...
    https://medlineplus.gov/...milial-hemophagocytic-lymphohistiocytosis - Genetics
  9. Hereditary paraganglioma-pheochromocytoma 
    ... PubMed Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney ... Group. Distinct clinical features of paraganglioma syndromes associated with ...
    https://medlineplus.gov/...hereditary-paraganglioma-pheochromocytoma - Genetics
  10. SETBP1 gene 
    ... promotes the growth of cancers by allowing abnormal blood cells to grow and divide uncontrollably, although the exact mechanism is unknown. KIAA0437 SEB SET-binding protein SET-binding protein isoform a SET-binding protein isoform b SETBP_HUMAN Tests of SETBP1 PubMed SET-BINDING ...
    https://medlineplus.gov/genetics/gene/setbp1 - Genetics
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