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Clinical Genetics|March 1, 1976
Recurrence risks in a consecutive series of congenitally malformed children dying in the perinatal periodK H Gustavson, H JorulfHelvetica Paediatrica Acta|October 1, 1975
Different types of osteochondrodysplasia in a consecutive series of newbornsK H Gustavson, H JorulfUpsala Journal of Medical Sciences|January 1, 1988
Familial ovarian dermoid cystsK H Gustavson, C RuneHuman Heredity|January 1, 1984
Spatial distribution of the gene for infantile genetic agranulocytosisL Iselius, K H GustavsonSwedish Dental Journal|January 1, 1987
Malocclusions in physically and/or mentally handicapped childrenA Oreland, J Heijbel, S JagellHuman 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 WadeliusActa Ophthalmologica|June 1, 1980
Specific changes in the fundus typical for the Sjögren-Larsson syndrome. An ophthalmological study of 35 patientsS Jagell, W Polland, O SandgrenSwedish Dental Journal|January 1, 1983
Oral conditions in Sjögren-Larsson syndromeH Forsberg, S Jagell, C O ReutervingNeuroradiology|March 1, 1981
Cranial CT in the Sjögren-Larsson syndromeF P Probst, S Jagell, J HeijbelClinical Genetics|July 1, 1975
Bilateral teratoma of testis in two brothers with 47,XXY Klinefelter's syndromeK H Gustavson, I Gamstorp, S MeurlingPageof 14