Bakker E - Search Results

1

Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.

Oostra BA, Majoor-Krakauer DF, van Hemel JO, Bakker E, Callen DF, Schmidt M, van Oost BA. Oostra BA, et al. Among authors: bakker e. Am J Med Genet. 1991 Feb-Mar;38(2-3):332-5. doi: 10.1002/ajmg.1320380233. Am J Med Genet. 1991. PMID: 1673306

2

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.

van Oost BA, Smits A, Dreesen JC, Smeets D, Perdon L, van Bennekom CA, Dahl N, Bakker E, Oostra BA. van Oost BA, et al. Among authors: bakker e. Am J Med Genet. 1991 Feb-Mar;38(2-3):328-31. doi: 10.1002/ajmg.1320380232. Am J Med Genet. 1991. PMID: 2018075

3

New polymorphic DNA marker close to the fragile site FRAXA.

Oostra BA, Hupkes PE, Perdon LF, van Bennekom CA, Bakker E, Halley DJ, Schmidt M, Du Sart D, Smits A, Wieringa B, et al. Oostra BA, et al. Among authors: bakker e. Genomics. 1990 Jan;6(1):129-32. doi: 10.1016/0888-7543(90)90457-6. Genomics. 1990. PMID: 1968042 Free article.

4

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL. Bakker E, et al. J Med Genet. 1986 Dec;23(6):573-80. doi: 10.1136/jmg.23.6.573. J Med Genet. 1986. PMID: 2879929 Free PMC article.

5

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

Losekoot M, Hoogendoorn E, Olmer R, Jansen CC, Oosterwijk JC, van den Ouweland AM, Halley DJ, Warren ST, Willemsen R, Oostra BA, Bakker E. Losekoot M, et al. Among authors: bakker e. J Med Genet. 1997 Nov;34(11):924-6. doi: 10.1136/jmg.34.11.924. J Med Genet. 1997. PMID: 9391887 Free PMC article.

6

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: bakker e. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

7

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

Breuning MH, Snijdewint FG, Dauwerse JG, Saris JJ, Bakker E, Pearson PL, vanOmmen GJ. Breuning MH, et al. Among authors: bakker e. J Med Genet. 1990 Oct;27(10):614-7. doi: 10.1136/jmg.27.10.614. J Med Genet. 1990. PMID: 1978861 Free PMC article.

8

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

Veenema H, Carpenter NJ, Bakker E, Hofker MH, Ward AM, Pearson PL. Veenema H, et al. Among authors: bakker e. J Med Genet. 1987 Jul;24(7):413-21. doi: 10.1136/jmg.24.7.413. J Med Genet. 1987. PMID: 2886667 Free PMC article.

9

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

Bröcker-Vriends AH, Rosendaal FR, van Houwelingen JC, Bakker E, van Ommen GJ, van de Kamp JJ, Briët E. Bröcker-Vriends AH, et al. Among authors: bakker e. J Med Genet. 1991 Oct;28(10):672-80. doi: 10.1136/jmg.28.10.672. J Med Genet. 1991. PMID: 1682494 Free PMC article.

10

Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.

Deutz-Terlouw PP, Losekoot M, Olmer R, Pieneman WC, de Vries-v d Weerd S, Briët E, Bakker E. Deutz-Terlouw PP, et al. Among authors: bakker e. J Med Genet. 1995 Apr;32(4):296-300. doi: 10.1136/jmg.32.4.296. J Med Genet. 1995. PMID: 7643361 Free PMC article.

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