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Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A case of term mors in utero in a chromosome 11p linked long QT syndrome familyS Desmyttere, M Bonduelle, D De Wolf, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Apert syndrome, an antenatal ultrasound detected caseP Parent, H Le Guern, M R Munck, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Fluorescence in situ hybridisation on formalin fixed fetal tissue in the diagnosis of chromosomal syndromesJ M Cobben, C E Essed, J Hirdes, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parentsC Stoll, Y Alembik, P LutzGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French familyG Lucotte, S Berriche, F David, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Paternal line of transmission in chorea of Huntington with very early onsetC Navarrete, I Martinez, F SalamancaGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidusH Santos, I Cordeiro, A Medeira, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Fraser (Cryptophthalmos-syndactyly) syndrome: a case with bilateral anophthalmia but presence of normal eyelidsR Pankau, C J Partsch, U Jänig, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
46,XY/48,XYYY mosaicism case report and review of the literatureM Teyssier, G PoussetGenetic Counseling (Geneva, Switzerland)|January 1, 1994
A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological featuresA M Wiegers, L M Curfs, H Meijer, et al.Pageof 116