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Annales De Genetique|April 2, 2003
Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndromeArabella Smith, Lisa Robson, Luke St HeapsAnnales De Genetique|April 2, 2003
Auricular mild errors of morphogenesis: epidemiological study with application of a targeted computer programMarta Grun, Paul Merlob, Andrei Grunfeld, et al.Annales De Genetique|June 1, 1975
A family with three sibs carrying trisomy 21F Nuzzo, M Stefanini, G Simoni, et al.Annales De Genetique|June 24, 2003
Mucopolysaccharidosis I: a comparative study of haplotypes Eco47III-NspI sites frequencies in patients and healthy subjects of Mexican populationM P Gallegos-Arreola, L Arnaud-López, L E Figuera, et al.Annales De Genetique|June 24, 2003
A patient with hydranencephaly and PEHO-like dysmorphic featuresCyril Goizet, Caroline Espil-Taris, Marie Husson, et al.Annales De Genetique|June 24, 2003
Severe psychomotor retardation in a boy with a supernumerary derivative chromosome resulting in partial trisomy 21 and partial trisomy 7pBodil Edman Ahlbom, Jan Wahlström, Robert Saalman, et al.Annales De Genetique|June 24, 2003
Disease associated balanced chromosome rearrangements (DBCR): report of two new casesV S Tonk, H E Wyandt, X Huang, et al.Annales De Genetique|January 1, 1984
[Unstained chromosomes. A simple method for observation]J Lejeune, M O Rethoré, M C de Blois, et al.Annales De Genetique|January 1, 1980
A simple screening procedure for adenylate kinase, hexokinase and glucose-6-phosphate dehydrogenase deficienciesG Vaca, J Sanchez-Corona, N Olivares, et al.Annales De Genetique|January 1, 1983
Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literatureK Taysi, W T Chao, N Monaghan, et al.Pageof 129