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Annales De Genetique|January 1, 1989
Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotypeJ P Fryns, A Kleczkowska, H Kenis, et al.Annales De Genetique|January 1, 1989
Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second exampleJ P Fryns, A Kleczkowska, J Jaeken, et al.Annales De Genetique|January 1, 1988
Genetic counselling, carrier detection, and prenatal diagnosis in hemophilia. A service experienceJ Kaplan, M L Chauvet, M L Briard, et al.Annales De Genetique|January 1, 1988
Aplasia of the thumbs and great toes as the outstanding feature of Yunis and Varon syndrome. A new entity. A new observationR A Pfeiffer, L Diekmann, H J StockAnnales De Genetique|January 1, 1988
[Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]B Le Marec, S Odent, E Bracq, et al.Annales De Genetique|January 1, 1988
Deletion 1q42.3----qter in a girl with psychomotoric retardation and multiple dysmorphismsK Kausch, J Köhler, M SchmidAnnales De Genetique|January 1, 1988
Interstitial deletion of 17p11.2: case report and reviewM A Hamill, S H Roberts, M J Maguire, et al.Annales De Genetique|January 1, 1988
Poor prognosis of acute lymphoblastic leukemia with translocation (1;19) in childhood: potential interest of allogeneic bone marrow transplantationA M Vagner-Capodano, G Michel, D Maraninchi, et al.Annales De Genetique|January 1, 1988
The fetal phenotype of the 18p-syndrome. Report of a male fetus at twenty-one weeksH Göcke, I Muradow, W SteinAnnales De Genetique|January 1, 1979
An infertile male with balanced Y;19 translocation. Review of Y;autosome translocationsA Smith, I S Fraser, G ElliottPageof 129