Breedveld G - Search Results

1

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

Di Fonzo A, Rohé CF, Ferreira J, Chien HF, Vacca L, Stocchi F, Guedes L, Fabrizio E, Manfredi M, Vanacore N, Goldwurm S, Breedveld G, Sampaio C, Meco G, Barbosa E, Oostra BA, Bonifati V; Italian Parkinson Genetics Network. Di Fonzo A, et al. Among authors: breedveld g. Lancet. 2005 Jan 29-Feb 4;365(9457):412-5. doi: 10.1016/S0140-6736(05)17829-5. Lancet. 2005. PMID: 15680456

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: breedveld gj. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

3

Genetic study on Tourette syndrome in The Netherlands.

Heutink P, van de Wetering BJ, Breedveld GJ, Oostra BA. Heutink P, et al. Among authors: breedveld gj. Adv Neurol. 1992;58:167-72. Adv Neurol. 1992. PMID: 1414621 Review. No abstract available.

4

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: breedveld gj. 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.

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: breedveld g. 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: breedveld gj. 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: breedveld gj. 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

Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36.

Zguricas J, Heus H, Morales-Peralta E, Breedveld G, Kuyt B, Mumcu EF, Bakker W, Akarsu N, Kay SP, Hovius SE, Heredero-Baute L, Oostra BA, Heutink P. Zguricas J, et al. Among authors: breedveld g. J Med Genet. 1999 Jan;36(1):32-40. J Med Genet. 1999. PMID: 9950363 Free PMC article.

9

A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.

Heus HC, Hing A, van Baren MJ, Joosse M, Breedveld GJ, Wang JC, Burgess A, Donnis-Keller H, Berglund C, Zguricas J, Scherer SW, Rommens JM, Oostra BA, Heutink P. Heus HC, et al. Among authors: breedveld gj. Genomics. 1999 May 1;57(3):342-51. doi: 10.1006/geno.1999.5796. Genomics. 1999. PMID: 10329000

10

Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction.

Heus HC, Luijsterburg AJ, van Baren MJ, Breedveld GJ, Joosse MN, Nieuwenhuizen IM, Vermeij-Keers C, Oostra BA, Heutink P. Heus HC, et al. Among authors: breedveld gj. Mamm Genome. 2001 Jan;12(1):77-9. doi: 10.1007/s003350010235. Mamm Genome. 2001. PMID: 11178748 No abstract available.

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