These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
124 related articles for article (PubMed ID: 22043435)
1. Familial ectrodactyly syndrome in a nigerian child: a case report. Durowaye M; Adeboye M; Yahaya-Kongoila S; Adaje A; Adesiyun O; Ernest SK; Mokuolu OA; Adegboye A Oman Med J; 2011 Jul; 26(4):275-8. PubMed ID: 22043435 [TBL] [Abstract][Full Text] [Related]
4. Split-hand/feet malformation: A rare syndrome. Gane BD; Natarajan P J Family Med Prim Care; 2016; 5(1):168-9. PubMed ID: 27453866 [TBL] [Abstract][Full Text] [Related]
5. Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients. Elliott AM; Evans JA Am J Med Genet A; 2006 Jul; 140(13):1419-27. PubMed ID: 16688749 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate (EEC) syndrome without clefting: a rare case report. Malvankar DD; Sacchidanand S; Mallikarjun M Dermatol Online J; 2012 Feb; 18(2):5. PubMed ID: 22398226 [TBL] [Abstract][Full Text] [Related]
8. Pathogenesis of split-hand/split-foot malformation. Duijf PH; van Bokhoven H; Brunner HG Hum Mol Genet; 2003 Apr; 12 Spec No 1():R51-60. PubMed ID: 12668597 [TBL] [Abstract][Full Text] [Related]
9. Split hand and food deformity and the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC). A report of five patients. Schmidt R; Nitowsky HM Hum Genet; 1977 Nov; 39(1):15-25. PubMed ID: 924443 [TBL] [Abstract][Full Text] [Related]
11. Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada. Elliott AM; Reed MH; Chudley AE; Chodirker BN; Evans JA Am J Med Genet A; 2006 Jul; 140(13):1428-39. PubMed ID: 16673359 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of bilateral ectrodactyly and radial agenesis associated with trisomy 10 mosaicism. Lévy J; Jouannic JM; Saada J; Dhombres F; Siffroi JP; Portnoï MF Case Rep Genet; 2013; 2013():592702. PubMed ID: 23401811 [TBL] [Abstract][Full Text] [Related]
14. Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature. Paththinige CS; Sirisena ND; Escande F; Manouvrier S; Petit F; Dissanayake VHW BMC Med Genet; 2019 Jun; 20(1):108. PubMed ID: 31200655 [TBL] [Abstract][Full Text] [Related]
15. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting. Sorasio L; Biamino E; Garelli E; Ferrero GB; Silengo MC Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851 [TBL] [Abstract][Full Text] [Related]
18. Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred. Wallis CE Clin Genet; 1988 Oct; 34(4):252-7. PubMed ID: 3233778 [TBL] [Abstract][Full Text] [Related]
19. Dental and maxillofacial characteristics of six Japanese individuals with ectrodactyly-ectodermal dysplasia-clefting syndrome. Okamura E; Suda N; Baba Y; Fukuoka H; Ogawa T; Ohkuma M; Ahiko N; Yasue A; Tengan T; Shiga M; Tsuji M; Moriyama K Cleft Palate Craniofac J; 2013 Mar; 50(2):192-200. PubMed ID: 22236363 [TBL] [Abstract][Full Text] [Related]
20. Association of generalized aggressive periodontitis and ectrodactyly-ectodermal dysplasia-cleft syndrome. Joseph R; Nath SG Indian J Hum Genet; 2012 May; 18(2):259-62. PubMed ID: 23162310 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]