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Anaesthesia Reports|July 10, 2025
Association between joint dislocation and malignant hyperthermiaA O Gomes, P V Andrade, J M Santos, et al.Human Molecular Genetics|June 1, 1996
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3A L Sertié, M Quimby, E S Moreira, et al.Archives of General Psychiatry|June 1, 1980
Cerebral ventricular size and neuropsychological impairment in young chronic schizophrenics. Measurement by the standardized Luria-Nebraska Neuropsychological BatteryC J Golden, J A Moses, R Zelazowski, et al.Brain & Development|July 7, 1999
Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationU C Reed, A M Tsanaclis, M Vainzof, et al.Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.Molecular Psychiatry|October 14, 2000
Analysis of the disease risk locus DXS1047 polymorphism in Brazilian Alzheimer patientsA L Nishimura, J R Oliveira, S R Matioli, et al.International Journal of Radiation Oncology, Biology, Physics|March 1, 1986
Neurologic dysfunction in patients treated for small cell carcinoma of the lung: a clinical and radiological studyL Y Chak, L M Zatz, P Wasserstein, et al.European Journal of Human Genetics : EJHG|January 10, 2002
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumoursT S Zorick, Z Mustacchi, S Y Bando, et al.Genomics|April 1, 1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2pR Bashir, S Keers, T Strachan, et al.Pageof 26