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Human Heredity|January 1, 1984
Spatial distribution of the gene for infantile genetic agranulocytosisL Iselius, K H GustavsonClinical Genetics|July 1, 1975
Bilateral teratoma of testis in two brothers with 47,XXY Klinefelter's syndromeK H Gustavson, I Gamstorp, S MeurlingClinical Genetics|December 1, 1989
Hereditary spastic diplegia with mental retardation in two young siblingsK H Gustavson, K Modrzewska, A EriksonClinical Genetics|June 1, 1978
Prenatal diagnosis of an XXY foetal karyotype in a woman with a previous 21-trisomic childK H Gustavson, B Kjessler, S ThorénActa Paediatrica Scandinavica|May 1, 1988
Probable homozygotic form of the Marfan syndrome in a newborn childJ Schollin, B Bjarke, K H GustavsonClinical Genetics|February 1, 1984
Familial minor neurodevelopmental disordersF Rasmussen, K H Gustavson, B BilleClinical Genetics|February 1, 1983
Chromosomal breakage in multiple endocrine adenomatosis (types I and II)K H Gustavson, R Jansson, K ObergClinical Genetics|July 1, 1986
Paternal non-disjunction in a 46,XY/47,XXY individual with a fragile 17p12 in the motherN Tommerup, T Tønnesen, K H GustavsonClinical Genetics|October 1, 1981
A boy with true hermaphroditism and sex chromosome mosaicism and a fertile woman with Turner mosaicism in a family with a translocation 8p:19PG Annerén, T Frykberg, K H GustavsonUpsala Journal of Medical Sciences|January 1, 1981
Zinc and copper concentration in serum of patients with congenital ichthyosis, spastic di- or tetraplegia and mental retardation (Sjögren-Larsson syndrome)S Jagell, G Hallmans, K H GustavsonPageof 27