5 results for author:"Baxova A." in Literature citations
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| APOE epsilon4: a potential modulation factor in Rett syndrome. Zahorakova D., Jachymova M., Kemlink D., Baxova A., Martasek P. J. Child Neurol. 25:546-550(2010) · Mapped (5) |
| Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia. Campos-Xavier A.B., Martinet D., Bateman J., Belluoccio D., Rowley L., Tan T.Y., Baxova A., Gustavson K.H., Borochowitz Z.U., Innes A.M. et al. Am. J. Hum. Genet. 84:760-770(2009) · UniProtKB (2) · Mapped (1) |
| Antley-Bixler syndrome or POR deficiency? Tomkova M., Marohnic C.C., Baxova A., Martasek P. Cas. Lek. Cesk. 147:261-265(2008) · Mapped (9) |
| Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms. Zahorakova D., Rosipal R., Hadac J., Zumrova A., Bzduch V., Misovicova N., Baxova A., Zeman J., Martasek P. J. Hum. Genet. 52:342-348(2007) · Mapped (15) |
| Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. Mavrogiannis L.A., Antonopoulou I., Baxova A., Kutilek S., Kim C.A., Sugayama S.M., Salamanca A., Wall S.A., Morriss-Kay G.M., Wilkie A.O.M. Nat. Genet. 27:17-18(2001) · UniProtKB (1) |