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2. ADULT syndrome allelic to limb mammary syndrome (LMS)? Propping P; Friedl W; Wienker TF; Uhlhaas S; Zerres K Am J Med Genet; 2000 Jan; 90(2):179-82. PubMed ID: 10607963 [TBL] [Abstract][Full Text] [Related]
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4. A novel mutation (c.1010G>T; p.R337L) in TP63 as a cause of split-hand/foot malformation with hypodontia. Jin JY; Zeng L; Li K; He JQ; Pang X; Huang H; Xiang R; Tang JY J Gene Med; 2019 Oct; 21(10):e3122. PubMed ID: 31420900 [TBL] [Abstract][Full Text] [Related]
5. Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene. Rinne T; Spadoni E; Kjaer KW; Danesino C; Larizza D; Kock M; Huoponen K; Savontaus ML; Aaltonen M; Duijf P; Brunner HG; Penttinen M; van Bokhoven H Eur J Hum Genet; 2006 Aug; 14(8):904-10. PubMed ID: 16724007 [TBL] [Abstract][Full Text] [Related]
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9. Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype. Payne AS; Yan AC; Ilyas E; Li W; Seykora JT; Young TL; Pawel BR; Honig PJ; Camacho J; Imaizumi S; Heymann WR; Schnur RE Arch Dermatol; 2005 Dec; 141(12):1567-73. PubMed ID: 16365259 [TBL] [Abstract][Full Text] [Related]
10. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly. Berdón-Zapata V; Granillo-Alvarez M; Valdés-Flores M; García-Ortiz JE; Kofman-Alfaro S; Zenteno JC J Orthop Res; 2004 Jan; 22(1):1-5. PubMed ID: 14656652 [TBL] [Abstract][Full Text] [Related]
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12. TP63 mutation and clefting modifier genes in an EEC syndrome family. Ray AK; Marazita ML; Pathak R; Beever CL; Cooper ME; Goldstein T; Shaw DF; Field LL Clin Genet; 2004 Sep; 66(3):217-22. PubMed ID: 15324320 [TBL] [Abstract][Full Text] [Related]
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