Partial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1.
SourceEuropean Journal of Human Genetics, 13, 11, (2005), pp. 1169-71
Article / Letter to editor
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European Journal of Human Genetics
SubjectDCN 2: Functional Neurogenomics; IGMD 3: Genomic disorders and inherited multi-system disorders; IGMD 5: Health aging / healthy living; IGMD 9: Renal disorder; NCMLS 5: Membrane transport and intracellular motility; UMCN 1.2: Molecular diagnosis, prognosis and monitoring
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