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Community Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. ClementiPrenatal Diagnosis|April 5, 2001
Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in EuropeC Stoll, E Garne, M Clementi, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Rett-like syndrome in fragile X syndromeY Alembik, B Dott, C StollBlood|October 1, 1978
Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML)C Stoll, F Oberling, E FloriAnnales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B DottGenetic 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 LutzEuropean Journal of Pediatrics|May 18, 1979
A girl with an end-to-end fusion of two X'SC Stoll, C Lausecker, A PennerathVirchows Archiv : an International Journal of Pathology|December 16, 1998
The influence of p53 and associated factors on the outcome of patients with oral squamous cell carcinomaC Stoll, G Baretton, U LöhrsDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|August 11, 2007
[Injectable silicon--long term sequelae after use in plastic surgery]F Soost, C Stoll, P MeisterPageof 106