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Chromosoma|January 23, 1999
A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochoresA Wandall, L Tranebjaerg, N TommerupHereditas|January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22K Arheden, U Tantravahi, N Tommerup, et al.American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.Journal of Medical Genetics|February 1, 1987
New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20qM B Petersen, L Tranebjaerg, N Tommerup, et al.Ugeskrift for Laeger|June 13, 2000
[Genetic causes of hearing loss--status and perspectives]L TranebjaergTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|June 26, 1999
[Genetic causes of hearing loss--status and perspectives]L TranebjaergTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 3, 1999
[Genetic causes of mental retardation--diagnostic possibilities]L TranebjaergAnnales De Genetique|January 1, 1987
Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethalN TommerupHuman Genetics|January 1, 1982
Specific staining of 9h in human somatic interphase cells by D 287/170N TommerupHuman Genetics|March 1, 1989
Induction of the fragile X on BrdU-substituted chromosomes with direct visualization of sister chromatid exchanges on banded chromosomesN TommerupPageof 25