Eva Morava
University of Pécs
Medical Faculty
Department of Medical Genetics and Child Development
Pécs, 7623, Hungary
Hungary
Name/email consistency: high
- Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two families. Morava, E., Illés, T., Weisenbach, J., Kárteszi, J., Kosztolányi, G. Am. J. Med. Genet. A (2003)
- Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia. Morava, E., Bartsch, O., Czakó, M., Frensel, A., Kalscheuer, V., Kárteszi, J., Kosztolányi, G. Clin. Dysmorphol. (2003)
- Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome. Morava, E., Czakó, M., Kárteszi, J., Cser, B., Weissbecker, K., Méhes, K. Clin. Dysmorphol. (2003)
- A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion. Morava, E., Bartsch, O., Czako, M., Frensel, A., Kárteszi, J., Kosztolányi, G.Y. Genet. Couns. (2003)
- Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. Morava, E., Kárteszi, J., Weisenbach, J., Caliebe, A., Mundlos, S., Méhes, K. Eur. J. Pediatr. (2002)
- Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosis. Morava, E., Czakó, M., Aszmann, M., Illés, T., Kosztolányi, G.Y. Genet. Couns. (2002)
