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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1967 1
1975 1
1989 2
1992 1
1996 1
1997 1
1998 5
1999 2
2000 2
2002 1
2004 3
2008 1
2009 2
2010 1
2011 2
2012 1
2013 1
2020 1
2021 1
2024 0

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PubMed (cited) for id: 180297

28 results

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Page 1
A novel mutation in RHAG causing Rhnull phenotype in Colombia.
Junca TG, Pinilla JJ, Sanjuanelo M, Lopez K, Dezan MR, Peron AC, Oliveira VB, Conrado MCAV, Rocha V, Mendrone-Júnior A, Dinardo CL. Junca TG, et al. Transfusion. 2021 Sep;61(9):E62-E64. doi: 10.1111/trf.16596. Epub 2021 Jul 26. Transfusion. 2021. PMID: 34309026 No abstract available.
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.
Stewart AK, Shmukler BE, Vandorpe DH, Rivera A, Heneghan JF, Li X, Hsu A, Karpatkin M, O'Neill AF, Bauer DE, Heeney MM, John K, Kuypers FA, Gallagher PG, Lux SE, Brugnara C, Westhoff CM, Alper SL. Stewart AK, et al. Am J Physiol Cell Physiol. 2011 Dec;301(6):C1325-43. doi: 10.1152/ajpcell.00054.2011. Epub 2011 Aug 17. Am J Physiol Cell Physiol. 2011. PMID: 21849667 Free PMC article.
Generation and characterisation of Rhd and Rhag null mice.
Goossens D, Trinh-Trang-Tan MM, Debbia M, Ripoche P, Vilela-Lamego C, Louache F, Vainchenker W, Colin Y, Cartron JP. Goossens D, et al. Br J Haematol. 2010 Jan;148(1):161-72. doi: 10.1111/j.1365-2141.2009.07928.x. Epub 2009 Oct 5. Br J Haematol. 2010. PMID: 19807729 Free article.
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.
Fricke B, Jarvis HG, Reid CD, Aguilar-Martinez P, Robert A, Quittet P, Chetty M, Pizzey A, Cynober T, Lande WF, Mentzer WC, Düring M, Winter S, Delaunay J, Stewart GW. Fricke B, et al. Br J Haematol. 2004 Jun;125(6):796-803. doi: 10.1111/j.1365-2141.2004.04965.x. Br J Haematol. 2004. PMID: 15180870 Free article.
28 results