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American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.Ugeskrift for Laeger|July 22, 1991
[Minor head injuries in a Copenhagen district. 2. Causes, simultaneous lesions, alcohol and economic aspects]B R Duus, K B Nielsen, K V Kruse, et al.Human Genetics|August 1, 1991
The fragile X mutation does not have any major effect on the expression of the hypoxanthine phosphoribosyltransferase (HPRT) locus in human fibroblastsA M Steen, S Marcus, S Sahlén, et al.American Journal of Medical Genetics|January 1, 1991
Aicardi syndrome: early neuroradiological manifestations and results of DNA studies in one patientK B Nielsen, M Anvret, O Flodmark, et al.Human Genetics|October 19, 1978
Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndromeK B Nielsen, H Dyggve, U Friedrich, et al.The Journal of Biological Chemistry|November 25, 1989
Substitution of serine for alpha 1(I)-glycine 844 in a severe variant of osteogenesis imperfecta minimally destabilizes the triple helix of type I procollagen. The effects of glycine substitutions on thermal stability are either position of amino acid specificM Pack, C D Constantinou, K Kalia, et al.Human Genetics|January 1, 1983
Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile XK B Nielsen, N Tommerup, H Poulsen, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Cognitive development in offspring of untreated and preconceptionally treated maternal phenylketonuriaF Güttler, H Lou, J Andresen, et al.Scandinavian Journal of Respiratory Diseases|June 1, 1979
Resistive breathing training in severe chronic obstructive pulmonary disease. A pilot studyJ B Andersen, L Dragsted, T Kann, et al.Cytogenetics and Cell Genetics|January 1, 1997
Identification of positional candidates for neurological disorders on chromsome 13q14-->q22H G Nothwang, J Wirth, B Brandl, et al.Pageof 4