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Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.Human Genetics|December 1, 1986
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21M G Mattei, Y Colin, C Le Van Kim, et al.Journal De Genetique Humaine|June 1, 1989
[Linkage studies in Emery-Dreifuss muscular dystrophy]V Paquis, N Philip, M A Voelckel, et al.Medecine Tropicale : Revue Du Corps De Sante Colonial|February 9, 2007
[Drug supply for HIV patients in day care centre in Republic of Congo: the French Red Cross experience]C Libaudière, B Sibille, N Bakala, et al.The Journal of Cell Biology|March 1, 1986
Localization of the human NCAM gene to band q23 of chromosome 11: the third gene coding for a cell interaction molecule mapped to the distal portion of the long arm of chromosome 11C Nguyen, M G Mattei, J F Mattei, et al.Journal of Medical Screening|July 23, 2002
Outcome of a school screening programme for carriers of haemoglobin diseaseD Lena-Russo, C Badens, M Aubinaud, et al.Clinical Genetics|July 1, 1984
Cluster of acute infantile spinal muscular atrophy (Werdnig-Hoffmann disease) in a limited area of Reunion IslandM J Pascalet-Guidon, E Bois, J Feingold, et al.Prenatal Diagnosis|May 1, 1990
Socio-cultural inequities in access to prenatal diagnosis: the role of insurance coverage and regulatory policiesJ P Moatti, C Le Gales, C Julian, et al.Human Genetics|January 1, 1985
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosomeM G Mattei, N Philip, E Passage, et al.Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.Pageof 14