Losekoot M - Search Results

1

Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities.

Helderman-van den Enden AT, Maaswinkel-Mooij PD, Hoogendoorn E, Willemsen R, Maat-Kievit JA, Losekoot M, Oostra BA. Helderman-van den Enden AT, et al. Among authors: losekoot m. J Med Genet. 1999 Mar;36(3):253-7. J Med Genet. 1999. PMID: 10204857 Free PMC article.

2

Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis.

Losekoot M, van Heeren H, Schipper JJ, Giordano PC, Bernini LF, Fodde R. Losekoot M, et al. J Med Genet. 1992 Aug;29(8):574-7. doi: 10.1136/jmg.29.8.574. J Med Genet. 1992. PMID: 1355561 Free PMC article. No abstract available.

3

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.

Losekoot M, Fodde R, Harteveld CL, van Heeren H, Giordano PC, Went LN, Bernini LF. Losekoot M, et al. J Med Genet. 1991 Apr;28(4):252-5. doi: 10.1136/jmg.28.4.252. J Med Genet. 1991. PMID: 1856830 Free PMC article.

4

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: losekoot m. 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.

5

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.

De Rooij KE, De Koning Gans PA, Skraastad MI, Belfroid RD, Vegter-Van Der Vlis M, Roos RA, Bakker E, Van Ommen GJ, Den Dunnen JT, Losekoot M. De Rooij KE, et al. Among authors: losekoot m. J Med Genet. 1993 Dec;30(12):996-1002. doi: 10.1136/jmg.30.12.996. J Med Genet. 1993. PMID: 8133511 Free PMC article.

6

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. 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.

7

Predictive testing of 25 percent at-risk individuals for Huntington disease (1987-1997).

Maat-Kievit A, Vegter-Van Der Vlis M, Zoeteweij M, Losekoot M, van Haeringen A, Roos RA. Maat-Kievit A, et al. Among authors: losekoot m. Am J Med Genet. 1999 Dec 15;88(6):662-8. doi: 10.1002/(sici)1096-8628(19991215)88:6<662::aid-ajmg16>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10581487

8

Family history and DNA analysis in patients with suspected Huntington's disease.

Siesling S, Vegter-van de Vlis M, Losekoot M, Belfroid RD, Maat-Kievit JA, Kremer HP, Roos RA. Siesling S, et al. Among authors: losekoot m. J Neurol Neurosurg Psychiatry. 2000 Jul;69(1):54-9. doi: 10.1136/jnnp.69.1.54. J Neurol Neurosurg Psychiatry. 2000. PMID: 10864604 Free PMC article.

9

[From gene to disease; HD gene and Huntington disease].

Maat-Kievit JA, Losekoot M, Roos RA. Maat-Kievit JA, et al. Among authors: losekoot m. Ned Tijdschr Geneeskd. 2001 Nov 3;145(44):2120-3. Ned Tijdschr Geneeskd. 2001. PMID: 11723754 Review. Dutch.

10

Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease.

Maat-Kievit A, Helderman-van den Enden P, Losekoot M, de Knijff P, Belfroid R, Vegter-van der Vlis M, Roos R, Breuning M. Maat-Kievit A, et al. Among authors: losekoot m. Am J Med Genet. 2001 Dec 8;105(8):737-44. doi: 10.1002/ajmg.1610. Am J Med Genet. 2001. PMID: 11803522

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