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Results: 1-6 |
Results: 6

Authors: Sobacchi, C Frattini, A Orchard, P Porras, O Tezcan, I Andolina, M Babul-Hirji, R Baric, I Canham, N Chitayat, D Dupuis-Girod, S Ellis, I Etzioni, A Fasth, A Fisher, A Gerritsen, B Gulino, V Horwitz, E Klamroth, V Lanino, E Mirolo, M Musio, A Matthijs, G Nonomaya, S Notarangelo, LD Ochs, HD Furga, AS Valiaho, J van Hove, JLK Vihinen, M Vujic, D Vezzoni, P Villa, A
Citation: C. Sobacchi et al., The mutational spectrum of human malignant autosomal recessive osteopetrosis, HUM MOL GEN, 10(17), 2001, pp. 1767-1773

Authors: Johnson, JM Babul-Hirji, R Chitayat, D
Citation: Jm. Johnson et al., First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome, ULTRASOUN O, 17(4), 2001, pp. 344-346

Authors: Chitayat, D Babul-Hirji, R
Citation: D. Chitayat et R. Babul-hirji, Genetic counselling in prenatally diagnosed non-chromosomal fetal abnormalities, CUR OP OBST, 12(2), 2000, pp. 77-80

Authors: Gong, YQ Krakow, D Marcelino, J Wilkin, D Chitayat, D Babul-Hirji, R Hudgins, L Cremers, CW Cremers, FPM Brunner, HG Reinker, K Rimoin, DL Cohn, DH Goodman, FR Reardon, W Patton, M Francomano, CA Warman, ML
Citation: Yq. Gong et al., Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis, NAT GENET, 21(3), 1999, pp. 302-304

Authors: Allingham-Hawkins, SJ Babul-Hirji, R Chitayat, D Holden, JJA Yang, KT Lee, C Hudson, R Gorwill, H Nolin, SL Glicksman, A Jenkins, EC Brown, WT Howard-Peebles, PN Becchi, C Cummings, E Fallon, L Seitz, S Black, SH Vianna-Morgante, AM Costa, SS Otto, PA Mingroni-Netto, RC Murray, A Webb, J MacSwinney, F Dennis, N Jacobs, PA Syrrou, M Georgiou, I Patsalis, PC Uzielli, MLG Guarducci, S Lapi, E Cecconi, A Ricci, U
Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325

Authors: Gong, YQ Chitayat, D Kerr, B Chen, TP Babul-Hirji, R Pal, A Reiss, M Warman, ML
Citation: Yq. Gong et al., Brachydactyly type B: Clinical description, genetic mapping to chromosome 9q, and evidence for a shaved ancestral mutation, AM J HU GEN, 64(2), 1999, pp. 570-577
Risultati: 1-6 |