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Annales De Genetique|October 20, 1999
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.Annales De Genetique|October 20, 1999
Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresiaC H Wouters, T M van Bodegom, H A Moll, et al.Annales De Genetique|August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikelyK Eggermann, H A Wollmann, G Binder, et al.Annales De Genetique|January 1, 1994
IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-)D Gül, B S Sayli, F Gök, et al.Annales De Genetique|January 1, 1995
Chromosomal localization of two KOX zinc finger genes on chromosome bands 7q21-q22M F Rousseau-Merck, D Duro, R Berger, et al.Annales De Genetique|January 1, 1983
Protease inhibitor (PI) phenotype of individuals with chromosomal fragile sitesJ C Mulley, G R SutherlandAnnales De Genetique|January 1, 1983
[Fragility of the X chromosome and inhibition of dihydrofolate reductase. Comparison of the effects of 2 antibiotics: trimethoprim and pyrimethamine]M P Calva-Mercado, C Maunoury, M O Rethoré, et al.Annales De Genetique|January 1, 1983
[Absence of the palmar c triradius. Dermatoglyphic and geneologic study of a genetic character transmitted since the 17th century in a Quebec family]F B Genest, P GenestAnnales De Genetique|January 1, 1983
[Polymorphism of NOR bands in a normal French population]J E Dipierri, J FraisseAnnales De Genetique|January 1, 1983
Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemiaC Werner-Favre, C Cabrol, P Beris, et al.Pageof 129