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Ugeskrift for Laeger|December 21, 1992
[Genetic counseling. Past time, present time, future]K Brøndum-NielsenAmerican Journal of Medical Genetics|May 1, 1988
Growth pattern in boys with fragile XK Brøndum NielsenActa Paediatrica (Oslo, Norway : 1992). Supplement|December 24, 1997
The genetic basis for Prader-Willi syndrome: the importance of imprinted genesK Brøndum-NielsenClinical Genetics|September 1, 1996
Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft RegisterK Brøndum-Nielsen, K ChristensenPrenatal Diagnosis|July 1, 1995
A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samplesK Brøndum-Nielsen, M MikkelsenUgeskrift for Laeger|December 20, 1993
[Interphase cytogenetics--a new technique for analysis of acquired genetic changes in tumor cells]K Schousboe, K Brøndum-NielsenNordisk Medicin|January 1, 1993
[Prenatal diagnosis in Scandinavia]K Brøndum-Nielsen, B Nørgaard-PedersenUgeskrift for Laeger|June 26, 2001
[Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings]K Brøndum-Nielsen, M L PedersenHuman Genetics|May 26, 1998
Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutationsK Grønskov, A Hallberg, K Brøndum-NielsenUgeskrift for Laeger|September 28, 1998
[Fragile X syndrome. Diagnosis, genetics and clinical findings]H Hjalgrim, K Grønskov, K Brøndum-NielsenPageof 7