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Constant denaturant gel electrophoresis (CDGE) in BRCA1 mutation screening.
Andersen TI, Eiken HG, Couch F, Kaada G, Skrede M, Johnsen H, Aloysius TA, Tveit KM, Tranebjaerg L, Dørum A, Møller P, Weber BL, Børresen-Dale AL. Andersen TI, et al. Among authors: tranebjaerg l. Hum Mutat. 1998;11(2):166-74. doi: 10.1002/(SICI)1098-1004(1998)11:2<166::AID-HUMU10>3.0.CO;2-X. Hum Mutat. 1998. PMID: 9482581
Genetic services in Norway.
Tranebjaerg L, Børresen-Dale AL, Hansteen IL, Heim S, Kvittingen EA, Møller P. Tranebjaerg L, et al. Eur J Hum Genet. 1997;5 Suppl 2:130-4. Eur J Hum Genet. 1997. PMID: 9450210 No abstract available.
394delTT: a Nordic cystic fibrosis mutation.
Schwartz M, Anvret M, Claustres M, Eiken HG, Eiklid K, Schaedel C, Stolpe L, Tranebjaerg L. Schwartz M, et al. Among authors: tranebjaerg l. Hum Genet. 1994 Feb;93(2):157-61. doi: 10.1007/BF00210602. Hum Genet. 1994. PMID: 7509310
Mutation update on the CHD7 gene involved in CHARGE syndrome.
Janssen N, Bergman JE, Swertz MA, Tranebjaerg L, Lodahl M, Schoots J, Hofstra RM, van Ravenswaaij-Arts CM, Hoefsloot LH. Janssen N, et al. Among authors: tranebjaerg l. Hum Mutat. 2012 Aug;33(8):1149-60. doi: 10.1002/humu.22086. Epub 2012 Apr 16. Hum Mutat. 2012. PMID: 22461308 Review.
Spectrum of mutations in alpha-mannosidosis.
Berg T, Riise HM, Hansen GM, Malm D, Tranebjaerg L, Tollersrud OK, Nilssen O. Berg T, et al. Among authors: tranebjaerg l. Am J Hum Genet. 1999 Jan;64(1):77-88. doi: 10.1086/302183. Am J Hum Genet. 1999. PMID: 9915946 Free PMC article.
212 results