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Clinical manifestations of mitochondrial DNA depletion.
Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Among authors: chatkupt s. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728
Cerebellar infarction in children.
Chatkupt S, Epstein LG, Rappaport R, Koenigsberger MR. Chatkupt S, et al. Pediatr Neurol. 1987 Nov-Dec;3(6):363-6. doi: 10.1016/0887-8994(87)90009-9. Pediatr Neurol. 1987. PMID: 3508085
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
Brzustowicz LM, Allitto BA, Matseoane D, Theve R, Michaud L, Chatkupt S, Sugarman E, Penchaszadeh GK, Suslak L, Koenigsberger MR, et al. Brzustowicz LM, et al. Among authors: chatkupt s. Am J Hum Genet. 1994 Mar;54(3):482-8. Am J Hum Genet. 1994. PMID: 8116617 Free PMC article.
Reduced fecundity in male ALS gene-carriers.
Johnson WG, Lucek PR, Chatkupt S, Furman Y, Lustenberger A, Lazzarini A. Johnson WG, et al. Among authors: chatkupt s. Am J Med Genet. 1995 Nov 6;59(2):149-53. doi: 10.1002/ajmg.1320590206. Am J Med Genet. 1995. PMID: 8588576
20 results