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Clinical Genetics|May 1, 1985
A folate sensitive heritable fragile site at 19p13N Tommerup, J Nielsen, M MikkelsenHuman Genetics|January 1, 1981
X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriersK B Nielsen, N Tommerup, H Poulsen, 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.Human Genetics|January 1, 1983
Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile XK B Nielsen, N Tommerup, H Poulsen, et al.Human Genetics|October 1, 1993
Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephalyN Tommerup, E Mortensen, M H Nielsen, et al.Annales De Genetique|January 1, 1987
Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethalN TommerupBritish Journal of Cancer|May 1, 1996
Occurrence of cancer in women with Turner syndromeH Hasle, J H Olsen, J Nielsen, et al.Human 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 TommerupCytogenetics and Cell Genetics|January 1, 1984
Idoxuridine induction of micronuclei containing the long or short arms of human chromosome 9N TommerupPageof 222