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Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Renal tubular dysgenesis with hypoplastic calvaria: report of two casesS Erdogan, A Kacar, D Yilmazer, et al.Genetic Counseling (Geneva, Switzerland)|November 3, 2004
De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic featuresM Peippo, C Tengström, M Arvio, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large familyJ P Fryns, P Volcke, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphyC Stoll, S Finck, B Janser, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Minimal dysmorphic stigmata in 9q deletion of paternal originA Kleczkowska, J P Fryns, L Lemli, et al.Genetic Counseling (Geneva, Switzerland)|August 6, 2005
A case with de novo interstitial deletion of chromosome 7q21.1-q22E Manguoğlu, S Berker-Karaüzüm, A Baumer, et al.Genetic Counseling (Geneva, Switzerland)|August 6, 2005
Gingival fibromatosis, short stature, border-line IQ, facial dysmorphism and hepatomegalyI Marakoglu, E F Percin, U K Gursoy, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Wiedemann-Beckwith syndrome: clinical, cytogenetical and radiological observations in 39 new casesR Martínez y Martínez, R Martínez-Carboney, R Ocampo-Campos, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Smith-Lemli-Opitz syndrome: the changing phenotype with ageC de Die-Smulders, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 23, 1999
Length variations of the poly(T) tract at the exon 3 splice acceptor site of the choroideremia geneL Beaufrère, S Rieu, J C Hache, et al.Pageof 116