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X-linked myotubular myopathy in a female infant caused by a new MTM1 gene mutation.
Neurology. 2003 Apr 22;60(8):1363-5. doi: 10.1212/01.wnl.0000058763.90924.fa.
Neurology. 2003.
PMID: 12707446
Severe mucous membrane involvement in epidermolysis bullosa simplex with muscular dystrophy due to a novel plectin gene mutation.
Schara U, Tücke J, Mortier W, Nüsslein T, Rouan F, Pfendner E, Zillikens D, Bruckner-Tuderman L, Uitto J, Wiche G, Schröder R.
Schara U, et al. Among authors: tucke j.
Eur J Pediatr. 2004 Apr;163(4-5):218-22. doi: 10.1007/s00431-004-1410-4. Epub 2004 Feb 13.
Eur J Pediatr. 2004.
PMID: 14963703
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Latex type I sensitization and allergy in children with atopic dermatitis. Evaluation of cross-reactivity to some foods.
Tücke J, Posch A, Baur X, Rieger C, Raulf-Heimsoth M.
Tücke J, et al.
Pediatr Allergy Immunol. 1999 Aug;10(3):160-7. doi: 10.1034/j.1399-3038.1999.00013.x.
Pediatr Allergy Immunol. 1999.
PMID: 10565556
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Megalencephaly, mega corpus callosum, and complete lack of motor development: delineation of a rare syndrome.
Hengst M, Tücke J, Zerres K, Blaum M, Häusler M.
Hengst M, et al. Among authors: tucke j.
Am J Med Genet A. 2010 Sep;152A(9):2360-4. doi: 10.1002/ajmg.a.33577.
Am J Med Genet A. 2010.
PMID: 20803648
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