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Journal of Medical Genetics|February 1, 1979
Abnormal children of a 47,XYY fatherC Stoll, E Flori, A Clavert, et al.Genetic 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.Prenatal Diagnosis|April 1, 1994
Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesisD Satge, B Gasser, A Geneix, et al.Humangenetik|January 1, 1975
Ring chromosome 15:r(15). Identification by R bandingC Stoll, J G Juif, J C Luckel, et al.Prenatal Diagnosis|January 1, 1991
Prenatal diagnosis of congenital myasthenia with arthrogryposis in a myasthenic motherC Stoll, M C Ehret-Mentre, A Treisser, et al.Annales De Genetique|January 5, 2002
Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across EuropeC De Vigan, N Baena, E Cariati, et al.Mund-, Kiefer- Und Gesichtschirurgie : MKG|August 5, 2004
[Chorioallantoic membrane of fertilized avian eggs as a substrate for assessment of cancerous invasiveness]T Laurin, U Schmitz, D Riediger, et al.European Journal of Epidemiology|November 1, 1993
The epidemiology of three serious cardiac defects. A joint study between five centresC Francannet, P A Lancaster, P Pradat, et al.Gene|June 3, 1997
Cloning and analysis of MART-1/Melan-A human melanoma antigen promoter regionsL H Butterfield, T C Stoll, R Lau, et al.Human Genetics|January 1, 1983
Reexamination of paternal age effect in Down's syndromeM P Roth, J Feingold, A Baumgarten, et al.Pageof 30