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Surgery, Gynecology & Obstetrics|December 1, 1977
Value of a follow-up study of recurrent carcinoma of the colon and rectumC A Ekman, J Gustavson, A HenningClinical 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 GustavsonExpert Opinion on Medical Diagnostics|March 14, 2013
Tissue microarrays and quantitative tissue-based image analysis as a tool for oncology biomarker and diagnostic developmentMarisa P Dolled-Filhart, Mark D GustavsonClinical Genetics|July 1, 1978
Apparently non-deleted ring-1 chromosome and extreme growth failure in a mentally retarded girlB Kjessler, K H Gustavson, A WigertzPageof 65