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Results 1 - 10 of 12 for Hb SS disease
  1. ... Epub 2003 Jan 9. Citation on PubMed Rust S, Rosier M, Funke H, Real J, Amoura Z, Piette JC, Deleuze JF, Brewer HB, Duverger N, Denefle P, Assmann G. Tangier disease is caused by mutations in the gene encoding ...
  2. ... S, Ochs HD, Urschel S, Belohradsky BH, Ugrinovic S, Kumararatne DS, Lawrence TC, ... disease-causing from risk-increasing TNFRSF13B variants in antibody ...
  3. ... is the most common form of sickle cell disease. This form is caused by a particular variant in the HBB gene that results in the production of an abnormal version of beta-globin called hemoglobin S (HbS). In people with this condition, hemoglobin S replaces ...
  4. ... skin (jaundice).In Hb Bart syndrome and HbH disease, a shortage of alpha-globin ... carry oxygen to the body's tissues. The substitution of Hb Bart or HbH ...
  5. ... skin (jaundice). In Hb Bart syndrome and HbH disease, a shortage of ... carry oxygen to the body's tissues. The substitution of Hb Bart or HbH ...
  6. ... PubMed Sotiriou E, Coku J, Tanji K, Huang HB, Hirano M, DiMauro S. The m.3244G>A mutation in mtDNA is ...
  7. ... Citation on PubMed Worth A, Thrasher AJ, Gaspar HB. Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype. Br J Haematol. 2006 Apr; ...
  8. ... A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA. The role of RELN in lissencephaly and neuropsychiatric disease. Am J Med Genet B Neuropsychiatr Genet. 2007 ...
  9. ... JB, Wegner J, Tiemeyer M, Aoki K; Undiagnosed Diseases Network; Scottish Genome Partnership; Nordgren A, Hammarsjo A, Duker AL, Rohena L, Hove HB, Ek J, Adams D, Tifft CJ, Onyekweli T, ...
  10. ... SMC, Borges V, Limongi JCP, Rocha MSG, Ferraz HB, de Carvalho Aguiar P. The ... DC, Sharma N, Camargos S, Cardoso F, Patel RC. Altered activation of protein ...
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