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Clinical 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 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 WigertzPediatric Radiology|June 19, 1978
Spondylometaphyseal dysplasia in two sibs of normal parentsK H Gustavson, G Holmgren, F ProbstThe American Journal of Otology|July 1, 1987
Familial Menière's disease: a genetic investigationL Birgerson, K H Gustavson, J StahlePageof 14