Oostra BA - Search Results

1

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

van Duijn CM, Dekker MC, Bonifati V, Galjaard RJ, Houwing-Duistermaat JJ, Snijders PJ, Testers L, Breedveld GJ, Horstink M, Sandkuijl LA, van Swieten JC, Oostra BA, Heutink P. van Duijn CM, et al. Among authors: oostra ba. Am J Hum Genet. 2001 Sep;69(3):629-34. doi: 10.1086/322996. Epub 2001 Jul 2. Am J Hum Genet. 2001. PMID: 11462174 Free PMC article.

2

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: oostra ba. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

3

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. Heutink P, et al. Among authors: oostra ba. J Med Genet. 1990 Jul;27(7):433-6. doi: 10.1136/jmg.27.7.433. J Med Genet. 1990. PMID: 2395161 Free PMC article.

4

Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?

Heutink P, van de Wetering BJ, Pakstis AJ, Kurlan R, Sandor P, Oostra BA, Sandkuijl LA. Heutink P, et al. Among authors: oostra ba. Am J Hum Genet. 1995 Aug;57(2):465-73. Am J Hum Genet. 1995. PMID: 7668273 Free PMC article.

5

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families.

Heutink P, van Schothorst EM, van der Mey AG, Bardoel A, Breedveld G, Pertijs J, Sandkuijl LA, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: oostra ba. Eur J Hum Genet. 1994;2(3):148-58. doi: 10.1159/000472358. Eur J Hum Genet. 1994. PMID: 7834274

6

Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

Heutink P, Haitjema T, Breedveld GJ, Janssen B, Sandkuijl LA, Bontekoe CJ, Westerman CJ, Oostra BA. Heutink P, et al. Among authors: oostra ba. J Med Genet. 1994 Dec;31(12):933-6. doi: 10.1136/jmg.31.12.933. J Med Genet. 1994. PMID: 7891375 Free PMC article.

7

Dinucleotide repeat polymorphism at D11S994 locus.

Bontekoe CJ, de Graaff E, Breedveld GJ, Oostra BA, Heutink P. Bontekoe CJ, et al. Among authors: oostra ba. Hum Mol Genet. 1993 Oct;2(10):1747. doi: 10.1093/hmg/2.10.1747. Hum Mol Genet. 1993. PMID: 8268942 No abstract available.

8

Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity alone.

Galjaard RJ, van der Ham LI, Posch NA, Dijkstra PF, Oostra BA, Hovius SE, Timmenga EJ, Sonneveld GJ, Hoogeboom AJ, Heutink P. Galjaard RJ, et al. Among authors: oostra ba. Am J Med Genet. 2001 Jan 22;98(3):256-62. doi: 10.1002/1096-8628(20010122)98:3<256::aid-ajmg1088>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11169564

9

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P. Njajou OT, et al. Among authors: oostra ba. Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038. Nat Genet. 2001. PMID: 11431687

10

X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.

Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P. Galjaard RJ, et al. Among authors: oostra ba. Eur J Hum Genet. 2001 Sep;9(9):653-8. doi: 10.1038/sj.ejhg.5200692. Eur J Hum Genet. 2001. PMID: 11571552 Review.

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