K H Gustavson|G Samuelson|M Söderberg - JoVE Visualize

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Prenatal 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.

Acta Ophthalmologica|April 1, 1992

Congenital glaucoma resulting from a chromosomal translocationK H Gustavson, L Berggren, B Svedberg, et al.

Clinical Genetics|October 1, 1985

Lethal and non-lethal diastrophic dysplasia. A study of 14 Swedish casesK H Gustavson, G Holmgren, S Jagell, et al.

Helvetica Paediatrica Acta|December 1, 1984

Delineation of a characteristic phenotype in distal trisomy 2qM Kyllerman, J Wahlström, B Westerberg, et al.

Clinical Genetics|November 1, 1983

Zellweger's cerebro-hepato-renal syndrome--variations in expressivity and in defects of bile acid synthesisJ Gustafsson, K H Gustavson, G Karlaganis, et al.

Clinical Genetics|April 1, 1986

Deleted ring chromosome 22 in a mentally retarded boyK H Gustavson, W Arancibia, U Eriksson, et al.

Acta Paediatrica Scandinavica|November 1, 1990

Severe mental retardation in Jordanian children. A retrospective studyS Janson, A Jayakoddy, A Abulaban, et al.

American Journal of Medical Genetics|January 1, 1986

Infantile autism and the fragile X. A Swedish multicenter studyJ Wahlström, C Gillberg, K H Gustavson, et al.

Scandinavian Journal of Haematology|January 1, 1983

Blastic phase of myeloproliferative syndrome coexisting with a malignant teratomaH Hagberg, K H Gustavson, C Sundström, et al.

Acta Paediatrica Scandinavica|May 1, 1977

Severe mental retardation in a Swedish county. I. Epidemiology, gestational age, birth weight and associated CNS handicaps in children born 1959--70K H Gustavson, B Hagberg, G Hagberg, et al.

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Showing results (41-50 of 264) with videos related to

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Pageof 27

Prenatal 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.

Acta Ophthalmologica|April 1, 1992

Congenital glaucoma resulting from a chromosomal translocationK H Gustavson, L Berggren, B Svedberg, et al.

Clinical Genetics|October 1, 1985

Lethal and non-lethal diastrophic dysplasia. A study of 14 Swedish casesK H Gustavson, G Holmgren, S Jagell, et al.

Helvetica Paediatrica Acta|December 1, 1984

Delineation of a characteristic phenotype in distal trisomy 2qM Kyllerman, J Wahlström, B Westerberg, et al.

Clinical Genetics|November 1, 1983

Zellweger's cerebro-hepato-renal syndrome--variations in expressivity and in defects of bile acid synthesisJ Gustafsson, K H Gustavson, G Karlaganis, et al.

Clinical Genetics|April 1, 1986

Deleted ring chromosome 22 in a mentally retarded boyK H Gustavson, W Arancibia, U Eriksson, et al.

Acta Paediatrica Scandinavica|November 1, 1990

Severe mental retardation in Jordanian children. A retrospective studyS Janson, A Jayakoddy, A Abulaban, et al.

American Journal of Medical Genetics|January 1, 1986

Infantile autism and the fragile X. A Swedish multicenter studyJ Wahlström, C Gillberg, K H Gustavson, et al.

Scandinavian Journal of Haematology|January 1, 1983

Blastic phase of myeloproliferative syndrome coexisting with a malignant teratomaH Hagberg, K H Gustavson, C Sundström, et al.

Acta Paediatrica Scandinavica|May 1, 1977

Severe mental retardation in a Swedish county. I. Epidemiology, gestational age, birth weight and associated CNS handicaps in children born 1959--70K H Gustavson, B Hagberg, G Hagberg, et al.

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