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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1957 | 1 |
1962 | 1 |
2020 | 1 |
2024 | 0 |
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Genotype-phenotype correlation in children with hereditary spherocytosis.
Br J Haematol. 2020 Nov;191(3):486-496. doi: 10.1111/bjh.16750. Epub 2020 May 20.
Br J Haematol. 2020.
PMID: 32436265
Free article.
Hereditary spherocytosis (HS) is a common inherited haemolytic anaemia attributed to disturbances in five different red cell membrane proteins. ...Patients with ANK1 and SPTB variants showed a similar clinical phenotype. Within each gene, variant type or loca …
Hereditary spherocytosis (HS) is a common inherited haemolytic anaemia attributed to disturbances in five different red cell m …
Hereditary spherocytosis in the neonatal period: diagnosis, incidence, and treatment.
SHAPIRO CM, JOSEPHSON AM, ROZENGVAIG S, KAUFFMAN A.
SHAPIRO CM, et al.
J Pediatr. 1957 Mar;50(3):308-14. doi: 10.1016/s0022-3476(57)80028-6.
J Pediatr. 1957.
PMID: 13406684
No abstract available.
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Ascertaining genetic carriers of hereditary spherocytosis by statistical analysis of multiple laboratory tests.
MACKINNEY AA Jr, MORTONNE, KOSOWER NS, SCHILLING RF.
MACKINNEY AA Jr, et al.
J Clin Invest. 1962 Mar;41(3):554-67. doi: 10.1172/JCI104509.
J Clin Invest. 1962.
PMID: 14467968
Free PMC article.
No abstract available.
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