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Journal of Mental Deficiency Research|September 1, 1983
Diagnosis of the fragile X syndrome (Martin-Bell syndrome). Clinical findings in 27 males with the fragile site at Xq28K B NielsenClinical Genetics|April 1, 1988
Aarskog syndrome in a Danish family: an illustration of the need for dysmorphology in paediatricsK B NielsenAmerican Journal of Medical Genetics|January 1, 1986
Sex chromosome aneuploidy in fragile X carriersK B NielsenJournal of Medical Genetics|June 1, 1982
Inherited partial X chromosome duplication in a mentally retarded maleK B Nielsen, F LangkjaerHuman Genetics|January 1, 1984
Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28. Results of folic acid treatment on fra(X) expressionK B Nielsen, N TommerupClinical Genetics|June 1, 1991
Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84E Blennow, K B NielsenUgeskrift for Laeger|May 31, 1993
[CPAP treatment of newborn infants. A historical review]K B Nielsen, J E PedersenCancer Genetics and Cytogenetics|August 1, 1985
Chromosomal studies in familial polyposis coliK B Nielsen, S Bülow, N TommerupHuman Genetics|February 1, 1988
Investigation of three XX males by cytogenetic and DNA analyses. Suggestion of Y chromosome inversion polymorphismK B Nielsen, M Schwartz, H SardemannPageof 4