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N Tommerup

Showing results (81-90 of 179) with videos related to

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Molecular and Cellular Endocrinology|November 6, 2001
Human FATE is a novel X-linked gene expressed in fetal and adult testisC Olesen, N J Larsen, A G Byskov, et al.
Prenatal Diagnosis|April 1, 1997
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissectionG Senger, I Chudoba, U Friedrich, 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.
The Journal of Biological Chemistry|June 6, 1998
Ciao 1 is a novel WD40 protein that interacts with the tumor suppressor protein WT1R W Johnstone, J Wang, N Tommerup, et al.
Leukemia|October 3, 2002
Detection of illegitimate rearrangements within the immunoglobulin light chain loci in B cell malignancies using end sequenced probesT S Poulsen, A N Silahtaroglu, C G Gisselø, et al.
Clinical Genetics|October 1, 1992
Ring chromosome 22 and neurofibromatosisN Tommerup, M Warburg, V Gieselmann, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32A D Børglum, T Flint, N Tommerup, 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.
European Journal of Human Genetics : EJHG|April 21, 2001
MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation patternJ B Nielsen, K F Henriksen, C Hansen, et al.
FEBS Letters|July 14, 1998
Human rab11a: transcription, chromosome mapping and effect on the expression levels of host GTP-binding proteinsP S Gromov, J E Celis, C Hansen, et al.
Pageof 18

Showing results (81-90 of 179) with videos related to

Sort By:
Pageof 18
Molecular and Cellular Endocrinology|November 6, 2001
Human FATE is a novel X-linked gene expressed in fetal and adult testisC Olesen, N J Larsen, A G Byskov, et al.
Prenatal Diagnosis|April 1, 1997
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissectionG Senger, I Chudoba, U Friedrich, 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.
The Journal of Biological Chemistry|June 6, 1998
Ciao 1 is a novel WD40 protein that interacts with the tumor suppressor protein WT1R W Johnstone, J Wang, N Tommerup, et al.
Leukemia|October 3, 2002
Detection of illegitimate rearrangements within the immunoglobulin light chain loci in B cell malignancies using end sequenced probesT S Poulsen, A N Silahtaroglu, C G Gisselø, et al.
Clinical Genetics|October 1, 1992
Ring chromosome 22 and neurofibromatosisN Tommerup, M Warburg, V Gieselmann, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32A D Børglum, T Flint, N Tommerup, 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.
European Journal of Human Genetics : EJHG|April 21, 2001
MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation patternJ B Nielsen, K F Henriksen, C Hansen, et al.
FEBS Letters|July 14, 1998
Human rab11a: transcription, chromosome mapping and effect on the expression levels of host GTP-binding proteinsP S Gromov, J E Celis, C Hansen, et al.
Pageof 18