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Page 1
Cutaneous clues for diagnosing X-chromosomal disorders.
Vreeburg M, Sallevelt SC, Stegmann AP, van Geel M, Detisch YJ, Schrander-Stumpel CT, van Steensel MA, Marcus-Soekarman D. Vreeburg M, et al. Among authors: marcus soekarman d. Clin Genet. 2014 Apr;85(4):328-35. doi: 10.1111/cge.12162. Epub 2013 Aug 14. Clin Genet. 2014. PMID: 23578112
Hyperechogenic fetal bowel: counseling difficulties.
Marcus-Soekarman D, Offermans J, Van den Ouweland AM, Mulder AL, Muntjewerff N, Vossen M, Kleijer W, Schrander-Stumpel C, Dooijes D. Marcus-Soekarman D, et al. Eur J Med Genet. 2005 Oct-Dec;48(4):421-5. doi: 10.1016/j.ejmg.2005.05.001. Eur J Med Genet. 2005. PMID: 16378926
Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome.
Steijlen PM, van Geel M, Vreeburg M, Marcus-Soekarman D, Spaapen LJ, Castelijns FC, Willemsen M, van Steensel MA. Steijlen PM, et al. Among authors: marcus soekarman d. Br J Dermatol. 2007 Dec;157(6):1225-9. doi: 10.1111/j.1365-2133.2007.08254.x. Epub 2007 Oct 18. Br J Dermatol. 2007. PMID: 17949453
XX male with sex reversal and a de novo 11;22 translocation.
Macville MV, Loneus WH, Marcus-Soekarman D, Huys EH, Schoenmakers EF, Schrank-Hacker A, Emanuel BS, Engelen JJ. Macville MV, et al. Among authors: marcus soekarman d. Am J Med Genet A. 2006 Sep 15;140(18):1973-7. doi: 10.1002/ajmg.a.31397. Am J Med Genet A. 2006. PMID: 16894539 Free PMC article. No abstract available.
Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.
van Steensel MA, Verstraeten VL, Frank J, Kelleners-Smeets NW, Poblete-Gutiérrez P, Marcus-Soekarman D, Bladergroen RS, Steijlen PM, van Geel M. van Steensel MA, et al. Among authors: marcus soekarman d. J Invest Dermatol. 2007 Mar;127(3):588-93. doi: 10.1038/sj.jid.5700592. Epub 2006 Nov 23. J Invest Dermatol. 2007. PMID: 17124507 Free article.
14 results