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Page 1
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.
Nevo syndrome.
Hilderink BG, Brunner HG. Hilderink BG, et al. Among authors: brunner hg. Clin Dysmorphol. 1995 Oct;4(4):319-23. doi: 10.1097/00019605-199510000-00007. Clin Dysmorphol. 1995. PMID: 8574422
Cutis marmorata telangiectatica congenita: report of 18 cases.
Gerritsen MJ, Steijlen PM, Brunner HG, Rieu P. Gerritsen MJ, et al. Among authors: brunner hg. Br J Dermatol. 2000 Feb;142(2):366-9. doi: 10.1046/j.1365-2133.2000.03311.x. Br J Dermatol. 2000. PMID: 10730777 Review.
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.
van Bokhoven H, Hamel BC, Bamshad M, Sangiorgi E, Gurrieri F, Duijf PH, Vanmolkot KR, van Beusekom E, van Beersum SE, Celli J, Merkx GF, Tenconi R, Fryns JP, Verloes A, Newbury-Ecob RA, Raas-Rotschild A, Majewski F, Beemer FA, Janecke A, Chitayat D, Crisponi G, Kayserili H, Yates JR, Neri G, Brunner HG. van Bokhoven H, et al. Among authors: brunner hg. Am J Hum Genet. 2001 Sep;69(3):481-92. doi: 10.1086/323123. Epub 2001 Jul 17. Am J Hum Genet. 2001. PMID: 11462173 Free PMC article.
498 results