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Page 1
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. Schutte BC, et al. Among authors: basart am. Am J Med Genet. 1999 May 21;84(2):145-50. doi: 10.1002/(sici)1096-8628(19990521)84:2<145::aid-ajmg11>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10323740
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.
Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Lidral AC, et al. Among authors: basart am. Am J Hum Genet. 1998 Aug;63(2):557-68. doi: 10.1086/301956. Am J Hum Genet. 1998. PMID: 9683588 Free PMC article.