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Genetic Counseling (Geneva, Switzerland)|January 13, 2000
A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndromeC Stoll, J Terzic, M FischbachCommunity 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.Blood|October 1, 1978
Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML)C Stoll, F Oberling, E FloriEuropean 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 MeisterFrontiers in Aging Neuroscience|March 23, 2026
Interconnected roles of astrocytes and the blood-brain barrier in Parkinson's disease: pathological evidence, mechanistic insights, and knowledge gapsAnna C Stoll, Ashley S HarmsGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Long term follow-up of two sibs with an autosomal recessive form of chrondrodysplasia punctata and epilepsyC Stoll, F Pauly, J P SteibPageof 30