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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1997
[From knowledge about risk to the regulation of exposures to ionizing radiation]R Masse, J L PasquierHuman Genetics|April 1, 1993
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20I Dorval, S Odent, P Jezequel, et al.Annales De Biologie Clinique|January 1, 1996
Fortuitous diagnosis of the association of hemoglobin J-Broussais with beta + thalassemiaM R Durou, A Ribault, M J Dufour, et al.Biochimica Et Biophysica Acta|April 11, 1986
Partial purification and characterization of a serine endopeptidase from rat liver plasma membranesL Guenet, F Gueble-Val, M Blayau, et al.Journal De Genetique Humaine|December 1, 1989
["Genetic emergencies" in a pediatric intensive care service]S Odent, P Betremieux, G Defawe, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A case of Larsen syndrome with severe cervical malformationsB Le Marec, M Chapuis, C Tréguier, et al.Prenatal Diagnosis|June 8, 2007
Embryology of neural tube defects: information provided by associated malformationsA S Cabaret, P Loget, L Loeuillet, et al.Journal of Medical Genetics|May 5, 1999
Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasiaS Odent, P Loget, B Le Marec, et al.Annales De Genetique|May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patientS Odent, S Taque, J Lucas, et al.Pageof 44