Niermeijer MF - Search Results

1

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: niermeijer mf. 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.

2

DNA analysis in patients with lissencephaly type I and other cortical dysplasias.

Oostra BA, de Rijk-van Andel JF, Eussen HJ, van Hemel JO, Halley DJ, Niermeijer MF. Oostra BA, et al. Among authors: niermeijer mf. Am J Med Genet. 1991 Sep 1;40(3):383-6. doi: 10.1002/ajmg.1320400328. Am J Med Genet. 1991. PMID: 1951447

3

The fragile X syndrome.

de Vries BB, Halley DJ, Oostra BA, Niermeijer MF. de Vries BB, et al. Among authors: niermeijer mf. J Med Genet. 1998 Jul;35(7):579-89. doi: 10.1136/jmg.35.7.579. J Med Genet. 1998. PMID: 9678703 Free PMC article. Review.

4

Benign hereditary chorea of early onset maps to chromosome 14q.

de Vries BB, Arts WF, Breedveld GJ, Hoogeboom JJ, Niermeijer MF, Heutink P. de Vries BB, et al. Among authors: niermeijer mf. Am J Hum Genet. 2000 Jan;66(1):136-42. doi: 10.1086/302725. Am J Hum Genet. 2000. PMID: 10631144 Free PMC article.

5

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.

Wessels MW, De Graaf BM, Cohen-Overbeek TE, Spitaels SE, de Groot-de Laat LE, Ten Cate FJ, Frohn-Mulder IF, de Krijger R, Bartelings MM, Essed N, Wladimiroff JW, Niermeijer MF, Heutink P, Oostra BA, Dooijes D, Bertoli-Avella AM, Willems PJ. Wessels MW, et al. Among authors: niermeijer mf. Hum Genet. 2008 Jan;122(6):595-603. doi: 10.1007/s00439-007-0436-x. Epub 2007 Oct 16. Hum Genet. 2008. PMID: 17938964

6

Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23.

de Vries BB, Breedveld GJ, Deelen WH, Breuning MH, Niermeijer MF, Heutink P. de Vries BB, et al. Among authors: niermeijer mf. Am J Med Genet. 2002 Sep 1;111(4):443-5. doi: 10.1002/ajmg.10576. Am J Med Genet. 2002. PMID: 12210308 No abstract available.

7

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: niermeijer mf. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

8

Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13.

De Rijk-van Andel JF, Catsman-Berrevoets CE, Halley DJ, Wesby-van Swaay E, Niermeijer MF, Oostra BA. De Rijk-van Andel JF, et al. Among authors: niermeijer mf. Hum Genet. 1991 Aug;87(4):509-10. doi: 10.1007/BF00197179. Hum Genet. 1991. PMID: 1879837

9

The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis.

Halley DJ, Veeze HJ, Sandkuyl LA, Wesby-van Swaay E, van Damme NH, Deelen WH, Witte JE, Niermeijer MF. Halley DJ, et al. Among authors: niermeijer mf. Hum Genet. 1990 Sep;85(4):407-8. doi: 10.1007/BF02428281. Hum Genet. 1990. PMID: 2210750

10

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.

van den Ouweland AM, de Vries BB, Bakker PL, Deelen WH, de Graaff E, van Hemel JO, Oostra BA, Niermeijer MF, Halley DJ. van den Ouweland AM, et al. Among authors: niermeijer mf. Am J Med Genet. 1994 Jul 15;51(4):482-5. doi: 10.1002/ajmg.1320510437. Am J Med Genet. 1994. PMID: 7943024

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

230 results

Search Page

Filters