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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1979 | 1 |
1988 | 1 |
1994 | 1 |
2024 | 0 |
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Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
Cell. 1994 Jun 17;77(6):869-80. doi: 10.1016/0092-8674(94)90136-8.
Cell. 1994.
PMID: 8004674
Localization of the McLeod locus (XK) within Xp21 by deletion analysis.
Bertelson CJ, Pogo AO, Chaudhuri A, Marsh WL, Redman CM, Banerjee D, Symmans WA, Simon T, Frey D, Kunkel LM.
Bertelson CJ, et al.
Am J Hum Genet. 1988 May;42(5):703-11.
Am J Hum Genet. 1988.
PMID: 3358422
Free PMC article.
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Hereditary acanthocytosis associated with the McLeod phenotype of the Kell blood group system.
Symmans WA, Shepherd CS, Marsh WL, Oyen R, Shohet SB, Linehan BJ.
Symmans WA, et al.
Br J Haematol. 1979 Aug;42(4):575-83. doi: 10.1111/j.1365-2141.1979.tb01170.x.
Br J Haematol. 1979.
PMID: 476009
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