Zeynep Tümer
Clinical Professor
1 - 5 out of 5Page size: 10
- 2009
- Published
Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
Tümer, Asuman Zeynep & Bach-Holm, D., Dec 2009, In: European Journal of Human Genetics. 17, 12, p. 1527-39 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A duplication encompassing the SHOX gene and the downstream evolutionarily conserved sequences
Roos, L., Brøndum Nielsen, K. & Tümer, Asuman Zeynep, 2009, In: American Journal of Medical Genetics. Part A. 149A, 12, p. 2900-1 1 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development
Zhang, L., Tümer, Asuman Zeynep, Møllgård, Kjeld, Barbi, G., Rossier, E., Bendsen, E., Møller, R. S., Ullmann, R., He, J., Papadopoulos, N., Tommerup, Niels & Larsen, Lars Allan, 2009, In: European Journal of Human Genetics.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genome-wide gene expression profiling of SCID mice with T-cell-mediated Colitis
Brudzewsky, D., Pedersen, Anders Elm, Claesson, Mogens Helweg, Gad, M., Kristensen, N. N., Lage, K., Jensen, T., Tommerup, Niels, Larsen, Lars Allan, Knudsen, S. & Tümer, Asuman Zeynep, 2009, In: Scandinavian Journal of Immunology. 69, 5, p. 437-46 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24
Hilhorst-Hofstee, Y., Tümer, Asuman Zeynep, Born, P., Knijnenburg, J., Hansson, K., Yatawara, V., Steensberg, J., Ullmann, R., Arkesteijn, G., Tommerup, Niels & Larsen, Lars Allan, 2009, In: American Journal of Medical Genetics. Part A. 149A, 8, p. 1830-3 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 7071
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Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
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1860
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
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Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans
Research output: Contribution to journal › Journal article › Research › peer-review
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