Showing results (11-20 of 690) with videos related to

Sort By:
Pageof 69
Human Genetics|August 1, 1997
A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of SwedenA Sillén, S Jagell, C Wadelius
Human Genetics|December 24, 1997
Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-telC Graff, T Jerndal, C Wadelius
American Journal of Medical Genetics|November 7, 1998
Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisationA Sillén, C Wadelius, G Annerén
Prenatal Diagnosis|February 19, 1998
First prenatal diagnosis by mutation analysis in a family with Sjögren-Larsson syndromeA Sillén, G Holmgren, C Wadelius
European Journal of Haematology|April 1, 1997
Venous thrombosis: factor V G1691A genotyping related to APC resistance as measured by 2 methodsA Alderborn, A Siegbahn, C Wadelius
Human Genetics|December 1, 1988
Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodiesC Wadelius, M Blombäck, U Pettersson
Acta Ophthalmologica|February 1, 1991
Lowe's oculocerebrorenal syndrome--variation in lens changes in the carrier stateP Fagerholm, G Annerén, C Wadelius
The Journal of Pediatrics|October 1, 1974
Urinary excretion of diphenylhydantoin metabolites in newborn infantsA Rane
Australian Family Physician|July 10, 1999
Incontinence in women. Don't suffer itA Rane
American Journal of Human Genetics|February 1, 1989
Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosisC Wadelius, P Fagerholm, U Pettersson, et al.
Pageof 69