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American Journal of Medical Genetics|February 1, 1991
How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: experience with first trimester chorionic villi samplingI Kennerknecht, G Barbi, N Dahl, et al.The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|June 2, 2022
Stool testing for pulmonary TB diagnosis in adultsL L Laursen, V N Dahl, C WejseActa Paediatrica Scandinavica|November 1, 1988
A case of complete trisomy 2p/triploidy mosaicismN Dahl, I L Eliasson, K H GustavsonHuman Genetics|September 1, 1997
Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22H Arnell, A Nemeth, G Annerén, et al.Clinical Genetics|October 1, 1996
Rapid detection of a mutation hot-spot in the human androgen receptorH Malmgren, J Gustavsson, T Tuvemo, et al.Archives of Orthopaedic and Trauma Surgery|January 1, 1992
Fracture patterns in malignant osteopetrosis (Albers-Schönberg disease)N Dahl, G Holmgren, S Holmberg, et al.Journal of Microscopy|March 6, 2013
Localizing and extracting filament distributions from microscopy imagesS Basu, K N Dahl, G K RohdePrenatal Diagnosis|July 1, 1992
Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type III (Norrbottnian type)N Dahl, C Wadelius, G Annerén, et al.Clinical Genetics|August 1, 1995
Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locusB E Ahlbom, N Dahl, P Zetterqvist, et al.Osteoarthritis and Cartilage|January 30, 2008
Familial osteochondritis dissecans associated with early osteoarthritis and disproportionate short statureE-L Stattin, Y Tegner, M Domellöf, et al.Pageof 14