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Detection of truncated dystrophin in fetal DMD myotubes.
Ginjaar IB, Bakker E, den Dunnen JT, Wessels A, van Paassen MM, Kloosterman MD, Zubrzycka-Gaarn EE, Fischbeck KH, Moorman AF, van Ommen GJ. Ginjaar IB, et al. Among authors: moorman af. Adv Exp Med Biol. 1990;280:17-23. doi: 10.1007/978-1-4684-5865-7_4. Adv Exp Med Biol. 1990. PMID: 2248137
Immunological study of dystrophin in Duchenne fetus.
Ginjaar IB, Bakker E, den Dunnen JT, van Paassen MM, van Ommen GJ, Zubrzycka-Gaarn E, Kloosterman MD, Wessels A, Moorman AF. Ginjaar IB, et al. Among authors: moorman af. Lancet. 1989 Nov 18;2(8673):1212-3. doi: 10.1016/s0140-6736(89)91813-8. Lancet. 1989. PMID: 2478851 No abstract available.
Fetal dystrophin to diagnose carrier status.
Ginjaar IB, Soffers S, Moorman AF, Nicholson LV, Morris GE, Bakker E, van Haeringen A, van Ommen GJ. Ginjaar IB, et al. Among authors: moorman af. Lancet. 1991 Jul 27;338(8761):258-9. doi: 10.1016/0140-6736(91)90402-b. Lancet. 1991. PMID: 1676813 No abstract available.
WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.
Stec I, Wright TJ, van Ommen GJ, de Boer PA, van Haeringen A, Moorman AF, Altherr MR, den Dunnen JT. Stec I, et al. Among authors: moorman af. Hum Mol Genet. 1998 Jul;7(7):1071-82. doi: 10.1093/hmg/7.7.1071. Hum Mol Genet. 1998. PMID: 9618163
374 results