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Results: 1-5 |
Results: 5

Authors: Vassal, H Medeira, A Cordeiro, I Santos, HG Castedo, S Saraiva, C da Silva, PM Monteiro, C
Citation: H. Vassal et al., Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Leri-Weill dyschondrosteosis, developmental delay, and ichthyosis, AM J MED G, 99(4), 2001, pp. 331-334

Authors: Harris, R Oliveira, JP Santos, HG
Citation: R. Harris et al., Formal recognition of the speciality of Medical Genetics in Portugal, EUR J HUM G, 8(1), 2000, pp. 3-3

Authors: Boerkoel, CF O'Neill, S Andre, JL Benke, PJ Bogdanovic, R Bulla, M Burguet, A Cockfield, S Cordeiro, I Ehrich, JHH Frund, S Geary, DF Ieshima, A Illies, F Joseph, MW Kaitila, I Lama, G Leheup, B Ludman, MD McLeod, DR Medeira, A Milford, DV Ormala, T Rener-Primec, Z Santava, A Santos, HG Schmidt, B Smith, GC Spranger, J Zupancic, N Weksberg, R
Citation: Cf. Boerkoel et al., Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature, EUR J PED, 159(1-2), 2000, pp. 1-7

Authors: Saraiva, JM Cordeiro, I Santos, HG
Citation: Jm. Saraiva et al., Robinow syndrome in monozygotic twins with normal stature, CLIN DYSMOR, 8(2), 1999, pp. 147-150

Authors: Oldridge, M Temple, IK Santos, HG Gibbons, RJ Mustafa, Z Chapman, KE Loughlin, J Wilkie, AOM
Citation: M. Oldridge et al., Brachydactyly type B: Linkage to chromosome 9q22 and evidence for genetic heterogeneity, AM J HU GEN, 64(2), 1999, pp. 578-585
Risultati: 1-5 |