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3. Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia. Tan AW; Leung P; Patil UP Fetal Pediatr Pathol; 2018 Aug; 37(4):296-300. PubMed ID: 30207817 [TBL] [Abstract][Full Text] [Related]
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6. Two distinct truncated variants of ankyrin associated with hereditary spherocytosis. Hayette S; Carré G; Bozon M; Alloisio N; Maillet P; Wilmotte R; Pascal O; Reynaud J; Reman O; Stéphan JL; Morlé L; Delaunay J Am J Hematol; 1998 May; 58(1):36-41. PubMed ID: 9590147 [TBL] [Abstract][Full Text] [Related]
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8. Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutations. Leite RC; Basseres DS; Ferreira JS; Alberto FL; Costa FF; Saad ST Hum Mutat; 2000 Dec; 16(6):529. PubMed ID: 11102985 [TBL] [Abstract][Full Text] [Related]
9. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis. Gallagher PG; Forget BG Blood Cells Mol Dis; 1998 Dec; 24(4):539-43. PubMed ID: 9887280 [No Abstract] [Full Text] [Related]
10. A previously unrecognized Ankyrin-1 mutation associated with Hereditary Spherocytosis in an Italian family. Lazzareschi I; Curatola A; Pedicelli C; Castiglia D; Buonsenso D; Gatto A; Attinà G; Valentini P Eur J Haematol; 2019 Nov; 103(5):523-526. PubMed ID: 31400153 [TBL] [Abstract][Full Text] [Related]
11. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis. Zhu F; Liang M; Xu L; Peng Z; Cai D; Wei X; Lin L; Shang X Gene; 2020 Feb; 726():144226. PubMed ID: 31669644 [TBL] [Abstract][Full Text] [Related]
12. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis. Gallagher PG; Ferreira JD; Costa FF; Saad ST; Forget BG Br J Haematol; 2000 Dec; 111(4):1190-3. PubMed ID: 11167760 [TBL] [Abstract][Full Text] [Related]
13. [Analysis of ANK1 gene mutation in a family with hereditary spherocytosis type Ⅰ]. Li D; Li B; Li S; Li W; Wang Y; Guo X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):999-1001. PubMed ID: 31598945 [TBL] [Abstract][Full Text] [Related]
14. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229 [TBL] [Abstract][Full Text] [Related]
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16. A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis? Bogusławska DM; Heger E; Listowski M; Wasiński D; Kuliczkowski K; Machnicka B; Sikorski AF Br J Haematol; 2014 Oct; 167(2):269-71. PubMed ID: 24903897 [No Abstract] [Full Text] [Related]
18. [COMBINED HEREDITARY SPHEROCYTOSIS AND ACQUIRED HEMOLYTIC ANEMIA]. MICHOT F Schweiz Med Wochenschr; 1963 Oct; 93():1500-2. PubMed ID: 14093393 [No Abstract] [Full Text] [Related]
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20. Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis. Lanciotti M; Perutelli P; Valetto A; Di Martino D; Mori PG Haematologica; 1997; 82(4):460-2. PubMed ID: 9299863 [No Abstract] [Full Text] [Related] [Next] [New Search]