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J Pediatr ; 139(3): 452-5, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11562629

ABSTRACT

We used a dual-color fluorescence in situ hybridization technique to estimate deleted mitochondrial DNA at a single-cell level and determine any correlation with the disease progression in lymphocytes from patients with Pearson marrow-pancreas syndrome. The method demonstrated a shift in heteroplasmy, paralleling the hematologic improvement.


Subject(s)
Anemia, Sideroblastic/genetics , DNA, Mitochondrial/blood , In Situ Hybridization, Fluorescence/methods , Pancreatic Diseases/genetics , Anemia, Sideroblastic/blood , Female , Hematopoietic Stem Cells/pathology , Humans , Infant , Lymphocytes , Pancreatic Diseases/blood , Syndrome
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