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kw.\*:("Syndrome Pearson")

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Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte culturesBOURGERON, T; CHRETIEN, D; RÖTIG, A et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 26, pp 19369-19376, issn 0021-9258Article

Pearson's marrow-pancreas syndrome : a multisystem mitochondrial disorder in infancyRÖTIG, A; CORMIER, V; MUNNICH, A et al.The Journal of clinical investigation. 1990, Vol 86, Num 5, pp 1601-1608, issn 0021-9738Article

Diagnosis and management of mitochondrial diseasesGILLIS, Lynette; KAYE, Edward.The Pediatric clinics of North America. 2002, Vol 49, Num 1, pp vii-viii, issn 0031-3955, 18 p.Article

Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndromeYANAGIHARA, Itaru; INUI, Koji; YANAGIBARA, Keiko et al.The Journal of pediatrics. 2001, Vol 139, Num 3, pp 452-455, issn 0022-3476Article

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