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P Moerman

Showing results (71-80 of 206) with videos related to

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Annales De Genetique|January 1, 1994
Neuroblastoma and partial 15q duplication in the fetusJ P Fryns, P Moerman, A Kleczkowska, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenitaP Moerman, J P Fryns, H Van Dijck, et al.
Journal De Genetique Humaine|September 1, 1989
[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]J P Fryns, P Moerman, H Van den Berghe, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 25, 1991
Intra-uterine Candida infection: a report of four infected fetusses from two mothersG G Donders, P Moerman, J Caudron, et al.
British Heart Journal|September 1, 1987
Interrupted right aortic arch in DiGeorge syndromeP Moerman, M Dumoulin, J Lauweryns, et al.
American Journal of Medical Genetics|October 1, 1988
Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observationE Legius, P Moerman, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The echographic diagnosis of fetal akinesia. A challenge towards etiological diagnosis and managementC Grubben, W Gyselaers, P Moerman, et al.
Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.
American Journal of Medical Genetics|January 23, 1999
Heterogeneity in omphalocoele with absent radial ray complexK Devriendt, J P Fryns, P Moerman, et al.
Pageof 21

Showing results (71-80 of 206) with videos related to

Sort By:
Pageof 21
Annales De Genetique|January 1, 1994
Neuroblastoma and partial 15q duplication in the fetusJ P Fryns, P Moerman, A Kleczkowska, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenitaP Moerman, J P Fryns, H Van Dijck, et al.
Journal De Genetique Humaine|September 1, 1989
[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]J P Fryns, P Moerman, H Van den Berghe, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 25, 1991
Intra-uterine Candida infection: a report of four infected fetusses from two mothersG G Donders, P Moerman, J Caudron, et al.
British Heart Journal|September 1, 1987
Interrupted right aortic arch in DiGeorge syndromeP Moerman, M Dumoulin, J Lauweryns, et al.
American Journal of Medical Genetics|October 1, 1988
Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observationE Legius, P Moerman, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The echographic diagnosis of fetal akinesia. A challenge towards etiological diagnosis and managementC Grubben, W Gyselaers, P Moerman, et al.
Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.
American Journal of Medical Genetics|January 23, 1999
Heterogeneity in omphalocoele with absent radial ray complexK Devriendt, J P Fryns, P Moerman, et al.
Pageof 21