AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Whiteford, ML Doig, WB Raine, PAM Hollman, AS Tolmie, JL
Citation: Ml. Whiteford et al., A new case of Myhre syndrome, CLIN DYSMOR, 10(2), 2001, pp. 135-140

Authors: Tobias, ES Patrick, WJA MacKenzie, JR Whiteford, ML
Citation: Es. Tobias et al., A case of Acro-renal-mandibular syndrome in an 18 week male fetus, CLIN DYSMOR, 10(1), 2001, pp. 61-64

Authors: Tyson, J Tranebjaerg, L McEntagart, M Larsen, LA Christiansen, M Whiteford, ML Bathen, J Aslaksen, B Sorland, SJ Lund, O Pembrey, ME Malcolm, S Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen (vol 107, pg 499, 2000), HUM GENET, 108(1), 2001, pp. 75-75

Authors: Tyson, J Tranebjaerg, L McEntagart, M Larsen, LA Christiansen, M Whiteford, ML Bathen, J Aslaksen, B Sorland, SJ Lund, O Pembrey, ME Malcolm, S Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen, HUM GENET, 107(5), 2000, pp. 499-503

Authors: Reid, E Dearlove, AM Whiteford, ML Rhodes, M Rubinsztein, DC
Citation: E. Reid et al., Autosomal dominant spastic paraplegia - Refined SPG8 locus and additional genetic heterogeneity, NEUROLOGY, 53(8), 1999, pp. 1844-1849

Authors: Tobias, ES Morrison, N Whiteford, ML Tolmie, JL
Citation: Es. Tobias et al., Towards earlier diagnosis of 22q11 deletions, ARCH DIS CH, 81(6), 1999, pp. 513-514
Risultati: 1-6 |