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26. New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1). The International Myotonic Dystrophy Consortium (IDMC). Neurology; 2000 Mar 28; 54(6):1218-21. PubMed ID: 10746587 [No Abstract] [Full Text] [Related]
27. DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus. Bi X, Xie H, Zheng H, Ding S, Zhang S, Wang Y, Xu Z, Ren D. Chin Med J (Engl); 2002 Nov 28; 115(11):1628-31. PubMed ID: 12609075 [Abstract] [Full Text] [Related]
28. Prenatal diagnosis of ornithine transcarbamylase deficiency with use of DNA polymorphisms. Fox J, Hack AM, Fenton WA, Golbus MS, Winter S, Kalousek F, Rozen R, Brusilow SW, Rosenberg LE. N Engl J Med; 1986 Nov 06; 315(19):1205-8. PubMed ID: 3762643 [No Abstract] [Full Text] [Related]
29. [A case of congenital myotonic dystrophy with hydrops fetalis]. Manabe A, Mori I, Fujimoto H, Tsunawaki A, Kondo Y. Nihon Sanka Fujinka Gakkai Zasshi; 1992 Dec 06; 44(12):1587-90. PubMed ID: 1484224 [No Abstract] [Full Text] [Related]
30. Experience in prenatal diagnosis of primary hyperoxaluria type 1. Rumsby G. J Nephrol; 1998 Dec 06; 11 Suppl 1():13-4. PubMed ID: 9604802 [Abstract] [Full Text] [Related]
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36. [A case of myotonic dystrophy diagnosed after delivery]. Yorinaga Y, Nishimura S, Ohara M. Nihon Sanka Fujinka Gakkai Zasshi; 1989 May 06; 41(5):613-6. PubMed ID: 2754292 [No Abstract] [Full Text] [Related]