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Molecular Syndromology|April 10, 2014
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 DeletionsC Dubourg, F Bonnet-Brilhault, A Toutain, et al.Southern Medical Journal|January 1, 1977
Ulnar nerve instability: ulnar nerve injury due to elbow flexionL LazaroComptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1980
[Isolation and physico-chemical properties of rat ceruloplasmin]B Legras, M R Durou, M Cottencin, et al.Human Genetics|August 1, 1990
HLA class I gene polymorphism in genetic hemochromatosisA M Jouanolle, J Yaouanq, M Blayau, et al.Journal of Hepatology|March 1, 1991
Short-term prednisolone followed by recombinant human alpha-interferon alone or combined with adenine-arabinoside in chronic hepatitis B. A prospective and randomized trialP Brissot, C Jacquelinet, H Jouanolle, et al.Prenatal Diagnosis|March 1, 1995
Serum lipid, apolipoprotein and lipoparticle levels in the human fetusB Legras, M R Durou, A Ruelland, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 16, 2011
Binder phenotype in mothers affected with autoimmune disordersE Colin, R Touraine, J M Levaillant, et al.Clinical Genetics|July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patientsE Chérot, B Keren, C Dubourg, et al.Cytogenetics and Cell Genetics|April 25, 2000
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseasesL Guenet, C Henry, B Toutain, et al.Diabetes & Metabolism|May 11, 2000
Determination of lipoprotein(a) concentrations and apolipoprotein(a) molecular weights in diabetic patientsA Ribault, M R Durou, C Letellier, et al.Pageof 44