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Presymptomatic diagnosis of myotonic dystrophy.
Brunner HG, Nillesen W, van Oost BA, Jansen G, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. J Med Genet. 1992 Nov;29(11):780-4. doi: 10.1136/jmg.29.11.780. J Med Genet. 1992. PMID: 1453426 Free PMC article.
Intestinal pseudo-obstruction in myotonic dystrophy.
Brunner HG, Hamel BC, Rieu P, Höweler CJ, Peters FT. Brunner HG, et al. J Med Genet. 1992 Nov;29(11):791-3. doi: 10.1136/jmg.29.11.791. J Med Genet. 1992. PMID: 1453429 Free PMC article.
Craniofrontonasal dysplasia.
Kapusta L, Brunner HG, Hamel BC. Kapusta L, et al. Among authors: brunner hg. Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936. Eur J Pediatr. 1992. PMID: 1468459
Molecular genetics of X-linked hearing impairment.
Brunner HG, Smeets B, Smeets D, Nelen M, Cremers CW, Ropers HH. Brunner HG, et al. Ann N Y Acad Sci. 1991;630:176-90. doi: 10.1111/j.1749-6632.1991.tb19586.x. Ann N Y Acad Sci. 1991. PMID: 1683204 Review. No abstract available.
Midline facial defects with ocular colobomata.
Temple IK, Brunner H, Jones B, Burn J, Baraitser M. Temple IK, et al. Am J Med Genet. 1990 Sep;37(1):23-7. doi: 10.1002/ajmg.1320370107. Am J Med Genet. 1990. PMID: 1700608
471 results