G. Grigelioniené
Paediatric Endocrinology Unit
Karolinska Hospital
Stockham
Sweden
Name/email consistency: high
- Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity. Grigelioniene, G., Schoumans, J., Neumeyer, L., Ivarsson, A., Eklöf, O., Enkvist, O., Tordai, P., Fosdal, I., Myhre, A.G., Westphal, O., Nilsson, N.O., Elfving, M., Ellis, I., Anderlid, B.M., Fransson, I., Tapia-Paez, I., Nordenskjöld, M., Hagenäs, L., Dumanski, J.P. Hum. Genet. (2001)
- Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia. Grigelioniene, G., Eklöf, O., Ivarsson, S.A., Westphal, O., Neumeyer, L., Kedra, D., Dumanski, J., Hagenäs, L. Hum. Genet. (2000)
- Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia. Grigelioniené, G., Eklöf, O., Laurencikas, E., Ollars, B., Hertel, N.T., Dumanski, J.P., Hagenäs, L. Acta Paediatr. (2000)
- A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. Online. Grigelioniené, G., Hagenäs, L., Eklöf, O., Neumeyer, L., Haereid, P.E., Anvret, M. Hum. Mutat. (1998)
