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Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. - Abstract - Europe PMC
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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
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Growth factor and receptor malfunctions associated with human genetic deafness - Naz - 2020 - Clinical Genetics - Wiley Online Library
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Growth factor and receptor malfunctions associated with human genetic deafness - Naz - 2020 - Clinical Genetics - Wiley Online Library
Growth factor and receptor malfunctions associated with human genetic deafness - Naz - 2020 - Clinical Genetics - Wiley Online Library
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