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Alica Baxová

First Faculty of Medicine, Charles University in Prague

3

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Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report

2018 BMC Nephrology
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Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia

2009 American Journal of Human Genetics
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Mutations of the homeobox gene ALX4 in parietal foramina and cranium bifidum: a component of DEFECT 11 syndrome.

2000 American Journal of Human Genetics
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