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Annales De Genetique|September 22, 2000
Progressive osseous heteroplasia: an uncommon cause of ossification of soft tissuesC Stoll, M R Javier, J P BellocqAnnales De Genetique|December 11, 1976
Duplication-deficiency of the short arm of chromosome 8 following artificial inseminationR G Weleber, R S Verma, W J Kimberling, et al.Annales De Genetique|December 1, 1976
Balanced translocations involving chromosome 12: report of a case and possible evidence for position effectB Biederman, P BowenAnnales De Genetique|November 6, 2001
A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotypingD Kotzot, H Holland, M Köhler, et al.Annales De Genetique|November 6, 2001
Heteromorphism 18ph+ : with or without reproductive consequences?A C Tabet, J M Dupont, A Lebbar, et al.Annales De Genetique|November 6, 2001
Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative availableM A Alcántara, R García-Cavazos, E Hernández-U, et al.Annales De Genetique|August 28, 2001
Cell-cycle kinetics of cell lines from patients with chromosomal mosaicismA Bortolai, M I MelaragnoAnnales De Genetique|August 28, 2001
Improved characterization of FSHD mutationsY Zhang, J Forner, S Fournet, et al.Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.Annales De Genetique|May 20, 2000
Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examinationC Stoll, B Dott, Y Alembik, et al.Pageof 129