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Position paper: Challenges and specific strategies for constitutional mismatch repair deficiency syndrome in low-resource settings.
Pediatr Blood Cancer. 2020 Aug;67(8):e28309. doi: 10.1002/pbc.28309. Epub 2020 May 30.
Pediatr Blood Cancer. 2020.
PMID: 32472748
Review.
Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.
Muralitharan S, Wali YA, Dennison D, Lamki ZA, Zachariah M, Nagwa el B, Pathare A, Krishnamoorthy R.
Muralitharan S, et al. Among authors: lamki za.
Am J Hematol. 2007 Dec;82(12):1099-102. doi: 10.1002/ajh.21009.
Am J Hematol. 2007.
PMID: 17674359
Free article.
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A prospective study of soft-tissue ultrasonography in sickle cell disease patients with suspected osteomyelitis.
William RR, Hussein SS, Jeans WD, Wali YA, Lamki ZA.
William RR, et al. Among authors: lamki za.
Clin Radiol. 2000 Apr;55(4):307-10. doi: 10.1053/crad.1999.0377.
Clin Radiol. 2000.
PMID: 10767192
Clinical Trial.
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