Merkx GF - Search Results

1

Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).

Koolen DA, Nillesen WM, Versteeg MH, Merkx GF, Knoers NV, Kets M, Vermeer S, van Ravenswaaij CM, de Kovel CG, Brunner HG, Smeets D, de Vries BB, Sistermans EA. Koolen DA, et al. Among authors: merkx gf. J Med Genet. 2004 Dec;41(12):892-9. doi: 10.1136/jmg.2004.023671. J Med Genet. 2004. PMID: 15591274 Free PMC article.

2

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.

Veltman JA, Schoenmakers EF, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, van Kessel AG. Veltman JA, et al. Am J Hum Genet. 2002 May;70(5):1269-76. doi: 10.1086/340426. Epub 2002 Apr 9. Am J Hum Genet. 2002. PMID: 11951177 Free PMC article.

3

A new case of dup(3q) syndrome due to a pure duplication of 3qter.

Faas BH, De Vries BB, Van Es-Van Gaal J, Merkx G, Draaisma JM, Smeets DF. Faas BH, et al. Clin Genet. 2002 Oct;62(4):315-20. doi: 10.1034/j.1399-0004.2002.620411.x. Clin Genet. 2002. PMID: 12372060

4

Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes.

Smeets DF, Merkx G. Smeets DF, et al. Hum Genet. 1990 Nov;86(1):76-8. doi: 10.1007/BF00205178. Hum Genet. 1990. PMID: 2253942

5

Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.

Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D. Kleefstra T, et al. Eur J Hum Genet. 2000 Aug;8(8):637-40. doi: 10.1038/sj.ejhg.5200500. Eur J Hum Genet. 2000. PMID: 10951526

6

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.

Van Der Burgt CJ, Merkx GF, Janssen AH, Mulder JC, Suijkerbuijk RF, Smeets DF. Van Der Burgt CJ, et al. Among authors: merkx gf. J Med Genet. 1992 Oct;29(10):739-41. doi: 10.1136/jmg.29.10.739. J Med Genet. 1992. PMID: 1433237 Free PMC article.

7

Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes.

Smeets DF, Merkx GF, Hopman AH. Smeets DF, et al. Among authors: merkx gf. Hum Genet. 1991 May;87(1):45-8. doi: 10.1007/BF01213090. Hum Genet. 1991. PMID: 2037282

8

A cytogenetic study in a large population of intellectually disabled Indonesians.

Mundhofir FE, Winarni TI, van Bon BW, Aminah S, Nillesen WM, Merkx G, Smeets D, Hamel BC, Faradz SM, Yntema HG. Mundhofir FE, et al. Genet Test Mol Biomarkers. 2012 May;16(5):412-7. doi: 10.1089/gtmb.2011.0157. Epub 2011 Dec 22. Genet Test Mol Biomarkers. 2012. PMID: 22191675 Free article.

9

Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14.

Faas BH, Van Der Deure J, Wunderink MI, Merkx G, Brunner HG. Faas BH, et al. Genet Couns. 2006;17(3):349-57. Genet Couns. 2006. PMID: 17100204

10

Evidence for specificity of the DA/DAPI technique.

Merkx GF, Hopman AH, Akkermans-Scholten AC, Smeets DF. Merkx GF, et al. Cytogenet Cell Genet. 1990;54(1-2):62-4. doi: 10.1159/000132957. Cytogenet Cell Genet. 1990. PMID: 1701116 No abstract available.

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

57 results

Search Page

Filters