Mulder M - Search Results

1

Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Groeneweg JA, Ummels A, Mulder M, Bikker H, van der Smagt JJ, van Mil AM, Homfray T, Post JG, Elvan A, van der Heijden JF, Houweling AC, Jongbloed JD, Wilde AA, van Tintelen JP, Hauer RN, Dooijes D. Groeneweg JA, et al. Among authors: mulder m. Heart Rhythm. 2014 Nov;11(11):2010-7. doi: 10.1016/j.hrthm.2014.07.041. Epub 2014 Jul 31. Heart Rhythm. 2014. PMID: 25087486

2

Nemaline myopathy caused byTNNT1 mutations in a Dutch pedigree.

van der Pol WL, Leijenaar JF, Spliet WG, Lavrijsen SW, Jansen NJ, Braun KP, Mulder M, Timmers-Raaijmakers B, Ratsma K, Dooijes D, van Haelst MM. van der Pol WL, et al. Among authors: mulder m. Mol Genet Genomic Med. 2014 Mar;2(2):134-7. doi: 10.1002/mgg3.52. Epub 2013 Dec 12. Mol Genet Genomic Med. 2014. PMID: 24689076 Free PMC article.

3

Search for copy number alterations in the MEFV gene using multiplex ligation probe amplification, experience from three diagnostic centres.

van Gijn ME, Soler S, de la Chapelle C, Mulder M, Ritorre C, Kriek M, Philibert L, van der Wielen M, Frenkel J, Grandemange S, Bakker E, Ploos van Amstel JK, Touitou I. van Gijn ME, et al. Among authors: mulder m. Eur J Hum Genet. 2008 Nov;16(11):1404-6. doi: 10.1038/ejhg.2008.135. Epub 2008 Jul 23. Eur J Hum Genet. 2008. PMID: 18648395

4

Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183).

Mulder MP, Wilke M, Langeveld A, Wilming LG, Hagemeijer A, van Drunen E, Zwarthoff EC, Riegman PH, Deelen WH, van den Ouweland AM, et al. Mulder MP, et al. Hum Genet. 1995 Aug;96(2):133-41. doi: 10.1007/BF00207368. Hum Genet. 1995. PMID: 7635459 Free article.

5

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

Van Hemel JO, Schaap C, Van Opstal D, Mulder MP, Niermeijer MF, Meijers JH. Van Hemel JO, et al. Among authors: mulder mp. J Med Genet. 1995 Aug;32(8):657-8. doi: 10.1136/jmg.32.8.657. J Med Genet. 1995. PMID: 7473663 Free PMC article.

6

Chromosome 12q heterozygosity is retained in i(12p)-positive testicular germ cell tumor cells.

Geurts van Kessel A, van Drunen E, de Jong B, Oosterhuis JW, Langeveld A, Mulder MP. Geurts van Kessel A, et al. Among authors: mulder mp. Cancer Genet Cytogenet. 1989 Jul 1;40(1):129-34. doi: 10.1016/0165-4608(89)90154-4. Cancer Genet Cytogenet. 1989. PMID: 2569358

7

Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region.

Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe BA, Groffen J. Heisterkamp N, et al. Among authors: mulder mp. Genomics. 1995 Sep 20;29(2):451-6. doi: 10.1006/geno.1995.9982. Genomics. 1995. PMID: 8666394

8

The octamer binding factor Oct6: cDNA cloning and expression in early embryonic cells.

Meijer D, Graus A, Kraay R, Langeveld A, Mulder MP, Grosveld G. Meijer D, et al. Among authors: mulder mp. Nucleic Acids Res. 1990 Dec 25;18(24):7357-65. doi: 10.1093/nar/18.24.7357. Nucleic Acids Res. 1990. PMID: 1979677 Free PMC article.

9

N- and KRAS mutations in primary testicular germ cell tumors: incidence and possible biological implications.

Olie RA, Looijenga LH, Boerrigter L, Top B, Rodenhuis S, Langeveld A, Mulder MP, Oosterhuis JW. Olie RA, et al. Among authors: mulder mp. Genes Chromosomes Cancer. 1995 Feb;12(2):110-6. doi: 10.1002/gcc.2870120205. Genes Chromosomes Cancer. 1995. PMID: 7535083 Free article.

10

Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential pyrimidine dimer site.

Keijzer W, Mulder MP, Langeveld JC, Smit EM, Bos JL, Bootsma D, Hoeijmakers JH. Keijzer W, et al. Among authors: mulder mp. Cancer Res. 1989 Mar 1;49(5):1229-35. Cancer Res. 1989. PMID: 2645048

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