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Clinical Genetics|April 1, 1991
Prader-Willi syndrome and Robertsonian translocations involving chromosome 15A C Casamassima, L R Shapiro, P L Wilmot, et al.Clinical Genetics|January 15, 2008
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegiaD V K Pantakani, U Zechner, L Arygriou, et al.Clinical Genetics|January 15, 2008
Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder populationM Plante, S Claveau, P Lepage, et al.Clinical Genetics|January 8, 2008
Familial Mediterranean Fever in Crete: a genetic and structural biological approach in a population of 'intermediate risk'E Fragouli, E Eliopoulos, E Petraki, et al.Clinical Genetics|January 8, 2008
Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand MaoriR V Port, J Arnold, D Kerr, et al.Clinical Genetics|January 8, 2008
Predictors of psychological distress among individuals with a strong family history of malignant melanomaN A Kasparian, B Meiser, P N Butow, et al.Clinical Genetics|January 8, 2008
Synpolydactyly: clinical and molecular advancesS Malik, K-H GrzeschikClinical Genetics|September 1, 1977
The foetus in Duchenne muscular dystrophy: muscle growth in tissue cultureA E Emery, L McGregorClinical Genetics|February 1, 1984
Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafnessJ Cornell, S Sellars, P BeightonClinical Genetics|February 1, 1984
Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosisS Canún, R M Lomelí, R Martínez, et al.Pageof 718