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Journal Abstract Search
163 related items for PubMed ID: 998189
21. Popliteal pterygium syndrome: a phenotypic and genetic analysis. Escobar V, Weaver D. J Med Genet; 1978 Feb; 15(1):35-42. PubMed ID: 633318 [Abstract] [Full Text] [Related]
22. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32. Lees MM, Winter RM, Malcolm S, Saal HM, Chitty L. J Med Genet; 1999 Dec; 36(12):888-92. PubMed ID: 10593995 [Abstract] [Full Text] [Related]
23. [Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)]. Pfeiffer RA, Verbeck C. Z Kinderheilkd; 1973 Oct 01; 115(3):235-44. PubMed ID: 4801123 [No Abstract] [Full Text] [Related]
25. Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders. Leslie EJ, O'Sullivan J, Cunningham ML, Singh A, Goudy SL, Ababneh F, Alsubaie L, Ch'ng GS, van der Laar IM, Hoogeboom AJ, Dunnwald M, Kapoor S, Jiramongkolchai P, Standley J, Manak JR, Murray JC, Dixon MJ. Am J Med Genet A; 2015 Mar 01; 167A(3):545-52. PubMed ID: 25691407 [Abstract] [Full Text] [Related]
26. Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene. Ghassibé M, Revencu N, Bayet B, Gillerot Y, Vanwijck R, Verellen-Dumoulin C, Vikkula M. J Med Genet; 2004 Feb 01; 41(2):e15. PubMed ID: 14757865 [No Abstract] [Full Text] [Related]
27. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome]. Szappanos L, Czeizel E, Szepesi K. Orv Hetil; 1984 Mar 11; 125(11):633-8. PubMed ID: 6700970 [No Abstract] [Full Text] [Related]
28. [The popliteal pterygium syndrome. A dominant autosomal malformation syndrome]. Pfeiffer RA, Tünte W, Reinken M. Z Kinderheilkd; 1970 Mar 11; 108(2):103-16. PubMed ID: 4325529 [No Abstract] [Full Text] [Related]
29. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate. Pegelow M, Koillinen H, Magnusson M, Fransson I, Unneberg P, Kere J, Karsten A, Peyrard-Janvid M. Cleft Palate Craniofac J; 2014 Jan 11; 51(1):49-55. PubMed ID: 23394314 [Abstract] [Full Text] [Related]
30. Multiple pterygium syndrome: mimicking the findings of Turner syndrome. Güven A, Kirmizibekmez H. J Pediatr Endocrinol Metab; 2011 Jan 11; 24(11-12):1089-93. PubMed ID: 22308873 [Abstract] [Full Text] [Related]
31. Popliteal pterygium syndrome in a Swedish family--clinical findings and genetic analysis with the van der Woude syndrome locus at 1q32-q41. Wong FK, Gustafsson B. Acta Odontol Scand; 2000 Apr 11; 58(2):85-8. PubMed ID: 10894430 [Abstract] [Full Text] [Related]
32. Popliteal pterygium syndrome with unusual features. Sasidharan CK, Ravi KV. Indian J Pediatr; 2004 Mar 11; 71(3):269-70. PubMed ID: 15080416 [Abstract] [Full Text] [Related]
33. Anatomic Severity, Midfacial Growth, and Speech Outcomes in Van der Woude/Popliteal Pterygium Syndromes Compared to Nonsyndromic Cleft Lip/Palate. Reardon JB, Brustowicz KA, Marrinan EM, Mulliken JB, Padwa BL. Cleft Palate Craniofac J; 2015 Nov 11; 52(6):676-81. PubMed ID: 25210863 [Abstract] [Full Text] [Related]
34. Phenotypic variation in the popliteal pterygium syndrome. Bixler D, Poland C, Nance WE. Clin Genet; 1973 Nov 11; 4(3):220-8. PubMed ID: 4203060 [No Abstract] [Full Text] [Related]
35. The popliteal pterygium syndrome: distinct phenotypic variation in two families. Hammer J, Kläusler M, Schinzel A. Helv Paediatr Acta; 1989 Jun 11; 43(5-6):507-14. PubMed ID: 2745146 [Abstract] [Full Text] [Related]
38. Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome. Kalay E, Sezgin O, Chellappa V, Mutlu M, Morsy H, Kayserili H, Kreiger E, Cansu A, Toraman B, Abdalla EM, Aslan Y, Pillai S, Akarsu NA. Am J Hum Genet; 2012 Jan 13; 90(1):76-85. PubMed ID: 22197489 [Abstract] [Full Text] [Related]
39. [Bilateral popliteal pterygium in siblings simultaneously affected with cleft lip and palate]. Standoli L, Gasperoni C. Minerva Chir; 1983 Mar 31; 38(6):393-6. PubMed ID: 6856124 [No Abstract] [Full Text] [Related]