Publication | Closed Access
Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome
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Citations
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References
2010
Year
Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesisGenetic EpidemiologyAlpers SyndromePathologyMolecular BiologyMolecular GeneticsDisease Gene IdentificationLarge Intragenic DeletionMolecular DiagnosticsOligonucleotide Array CghVariant InterpretationClinical Genetics
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