Rötig, A <br/><br/>
Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.  [electronic resource] 

 -  Genomics  Jun 1991 
 - 502-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1016/0888-7543(91)90342-c  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Bone Marrow--pathology<br/>Child<br/>Chromosome Deletion<br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Molecular Sequence Data<br/>Pancreatic Diseases--complications<br/>Pancytopenia--complications<br/>Polymerase Chain Reaction<br/>RNA<br/>Repetitive Sequences, Nucleic Acid<br/>Sequence Homology, Nucleic Acid<br/>Syndrome<br/>Vacuoles