Publication | Open Access
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
116
Citations
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References
2000
Year
Chromosome 6P25Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathologyMolecular GeneticsDisease Gene IdentificationAxenfeld-rieger SyndromeMedicineFkhl7 GeneVariant InterpretationClinical Genetics
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