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Clinical Genetics|April 1, 1986
Gonadoblastoma and Y-chromosome fluorescenceT Lukusa, J P Fryns, H van den BergheEuropean Journal of Pediatrics|December 1, 1986
Internal male pseudohermaphroditism in a 6 week old childT Lukusa, J P Fryns, H Van den BergheJournal De Genetique Humaine|May 1, 1987
[Sexual ambiguity and a non-fluorescent Y chromosome]J P Fryns, T Lukusa, R Vereecken, et al.Archives Francaises De Pediatrie|April 1, 1986
[Sexual ambiguity and non-fluorescent Y chromosome in 45,X/46,XY mosaicism]T Lukusa, J P Fryns, R Vereecken, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromesT Lukusa, J P Fryns, A Kleczkowska, et al.Human Genetics|September 1, 1991
"Spontaneous" FRA16B is a hot spot for sister chromatid exchangesT Lukusa, E Meulepas, J P Fryns, et al.Cancer Genetics and Cytogenetics|October 1, 1990
No significant increase in spontaneous and ethyl methane sulfonate-induced sister chromatid exchanges at the Xq27.3 fragile siteT Lukusa, E Meulepas, J P Fryns, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?J P Fryns, H Van Den BergheHuman Genetics|June 19, 1979
Congenital scalp defects associated with postaxial polydactylyJ P Fryns, H Van den BergheEuropean Journal of Pediatrics|June 28, 1979
Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?J P Fryns, H Van den BerghePageof 124