Feuth TB - Search Results

1

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers.

Spath MA, Feuth TB, Allen EG, Smits AP, Yntema HG, van Kessel AG, Braat DD, Sherman SL, Thomas CM. Spath MA, et al. Among authors: feuth tb. Hum Reprod. 2011 Aug;26(8):2185-91. doi: 10.1093/humrep/der146. Epub 2011 May 15. Hum Reprod. 2011. PMID: 21576079 Free PMC article.

2

X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers.

Spath MA, Nillesen WN, Smits AP, Feuth TB, Braat DD, van Kessel AG, Yntema HG. Spath MA, et al. Among authors: feuth tb. Am J Med Genet A. 2010 Feb;152A(2):387-93. doi: 10.1002/ajmg.a.33243. Am J Med Genet A. 2010. PMID: 20101683

3

Predictors and risk model development for menopausal age in fragile X premutation carriers.

Spath MA, Feuth TB, Smits AP, Yntema HG, Braat DD, Thomas CM, van Kessel AG, Sherman SL, Allen EG. Spath MA, et al. Among authors: feuth tb. Genet Med. 2011 Jul;13(7):643-50. doi: 10.1097/GIM.0b013e31821705e5. Genet Med. 2011. PMID: 21597380 Free PMC article.

4

Diagnostic genome profiling in mental retardation.

de Vries BB, Pfundt R, Leisink M, Koolen DA, Vissers LE, Janssen IM, Reijmersdal Sv, Nillesen WM, Huys EH, Leeuw Nd, Smeets D, Sistermans EA, Feuth T, van Ravenswaaij-Arts CM, van Kessel AG, Schoenmakers EF, Brunner HG, Veltman JA. de Vries BB, et al. Am J Hum Genet. 2005 Oct;77(4):606-16. doi: 10.1086/491719. Epub 2005 Aug 30. Am J Hum Genet. 2005. PMID: 16175506 Free PMC article.

5

Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.

Kooper AJ, Faas BH, Kater-Baats E, Feuth T, Janssen JC, van der Burgt I, Lotgering FK, van Kessel AG, Smits AP. Kooper AJ, et al. Prenat Diagn. 2008 Nov;28(11):1004-10. doi: 10.1002/pd.2111. Prenat Diagn. 2008. PMID: 18925610

6

Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplification.

Kooper AJA, Faas BHW, Feuth T, Creemers JWT, Zondervan HH, Boekkooi PF, Quartero RWP, Rijnders RJP, van der Burgt I, van Kessel AG, Smits APT. Kooper AJA, et al. J Mol Diagn. 2009 Jan;11(1):17-24. doi: 10.2353/jmoldx.2009.070140. Epub 2008 Dec 12. J Mol Diagn. 2009. PMID: 19074591 Free PMC article.

7

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, van Kessel AG, Schoenmakers EF, Veltman JA. Vissers LE, et al. Am J Hum Genet. 2003 Dec;73(6):1261-70. doi: 10.1086/379977. Epub 2003 Nov 18. Am J Hum Genet. 2003. PMID: 14628292 Free PMC article.

8

Why do parents prefer to know the fetal sex as part of invasive prenatal testing?

Kooper AJ, Pieters JJ, Eggink AJ, Feuth TB, Feenstra I, Wijnberger LD, Rijnders RJ, Quartero RW, Boekkooi PF, van Vugt JM, Smits AP. Kooper AJ, et al. Among authors: feuth tb. ISRN Obstet Gynecol. 2012;2012:524537. doi: 10.5402/2012/524537. Epub 2012 Dec 12. ISRN Obstet Gynecol. 2012. PMID: 23304540 Free PMC article.

9

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.

Koolen DA, Kramer JM, Neveling K, Nillesen WM, Moore-Barton HL, Elmslie FV, Toutain A, Amiel J, Malan V, Tsai AC, Cheung SW, Gilissen C, Verwiel ET, Martens S, Feuth T, Bongers EM, de Vries P, Scheffer H, Vissers LE, de Brouwer AP, Brunner HG, Veltman JA, Schenck A, Yntema HG, de Vries BB. Koolen DA, et al. Nat Genet. 2012 Apr 29;44(6):639-41. doi: 10.1038/ng.2262. Nat Genet. 2012. PMID: 22544363

10

Novel candidate tumour suppressor gene loci on chromosomes 11q23-24 and 22q13 involved in human insulinoma tumourigenesis.

Jonkers YM, Claessen SM, Feuth T, van Kessel AG, Ramaekers FC, Veltman JA, Speel EJ. Jonkers YM, et al. J Pathol. 2006 Dec;210(4):450-8. doi: 10.1002/path.2072. J Pathol. 2006. PMID: 17068744

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