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American Journal of Medical Genetics. Supplement|January 1, 1986
Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescenceB Hagberg, I Witt-EngerströmThe Journal of Pediatrics|August 1, 1978
Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantarisB Björkstén, K H Gustavson, B Eriksson, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit geneA Sillén, C Wadelius, M Sundvall, et al.Brain & Development|January 1, 1990
The Rett syndrome: gross motor disability and neural impairment in adultsI Witt-Engerström, B HagbergCancer Genetics and Cytogenetics|May 1, 1990
Benign ovarian teratomas. An analysis of their cellular originN Dahl, K H Gustavson, C Rune, et al.Clinical Genetics|September 1, 1984
Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variationsG Annerén, B Arvidson, K H Gustavson, et al.Acta Paediatrica Scandinavica|November 1, 1985
Selenium supplementation in X-linked muscular dystrophy. Effects on erythrocyte and serum selenium and on erythrocyte glutathione peroxidase activityM Gebre-Medhin, K H Gustavson, I Gamstorp, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|August 1, 1993
Early child health in Lahore, Pakistan: II. InbreedingM Yaqoob, K H Gustavson, F Jalil, et al.Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.Brain & Development|January 1, 1990
Early stages of the Rett syndrome and infantile neuronal ceroid lipofuscinosis--a difficult differential diagnosisB Hagberg, I Witt-EngerströmPageof 27