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Results: 1-4 |
Results: 4

Authors: Najmabadi, H Karimi-Nejad, R Sahebjam, S Pourfarzad, F Teimourian, S Sahebjam, F Amirizadeh, N Karimi-Nejad, MH
Citation: H. Najmabadi et al., The beta-thalassemia mutation spectrum in the Iranian population, HEMOGLOBIN, 25(3), 2001, pp. 285-296

Authors: Lagerstedt, K Carlberg, BM Karimi-Nejad, R Kleijer, WJ Bondeson, ML
Citation: K. Lagerstedt et al., Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): Identification of a fusion transcript including sequences from the gene W and the IDS gene, HUM MUTAT, 15(4), 2000, pp. 324-331

Authors: Feleki, X Najmabadi, H Karimi-Nejad, R Christopoulos, G Kleanthous, M
Citation: X. Feleki et al., Identification of a novel beta(0)-thalassemia mutation, codons 80/81 (-C),in an Iranian family, HEMOGLOBIN, 24(4), 2000, pp. 319-321

Authors: Shafeghati, Y Karimi-Nejad, A Karimi-Nejad, R
Citation: Y. Shafeghati et al., Supernumerary nipples in a Bartsocas-Papas patient in a consanguineous Iranian family, CLIN DYSMOR, 8(2), 1999, pp. 155-156
Risultati: 1-4 |