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Journal Abstract Search

232 related items for PubMed ID: 22197489

  • 21.
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  • 24. A case of facio-genito-popliteal syndrome.
    Hamamoto J, Matsumoto T.
    Ann Plast Surg; 1984 Sep; 13(3):224-9. PubMed ID: 6093671
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  • 25.
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  • 26. [Popliteal pterygium syndrome. A exceptional case].
    Brun MF, Delcampe P, Retout A, Bachy B, Peron JM.
    Rev Stomatol Chir Maxillofac; 1994 Sep; 95(5):343-7. PubMed ID: 7984954
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  • 29. Novel mutations in the IRF6 gene for Van der Woude syndrome.
    Wang X, Liu J, Zhang H, Xiao M, Li J, Yang C, Lin X, Wu Z, Hu L, Kong X.
    Hum Genet; 2003 Oct; 113(5):382-6. PubMed ID: 12920575
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  • 31. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
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  • 33. FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
    Simonis N, Migeotte I, Lambert N, Perazzolo C, de Silva DC, Dimitrov B, Heinrichs C, Janssens S, Kerr B, Mortier G, Van Vliet G, Lepage P, Casimir G, Abramowicz M, Smits G, Vilain C.
    J Med Genet; 2013 Sep; 50(9):585-92. PubMed ID: 23812909
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  • 34. The popliteal pterygium syndrome: an analysis of two families.
    Spauwen PH, Cobben JM, Gardeniers JW.
    J Craniomaxillofac Surg; 1994 Oct; 22(5):276-80. PubMed ID: 7798358
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  • 35. Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.
    Ben J, Jabs EW, Chong SS.
    Gene Expr Patterns; 2005 Jun; 5(5):629-38. PubMed ID: 15939375
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  • 36. Bartsocas-Papas syndrome with variable expressivity in an Egyptian family.
    Zaki MS, Kamel AK, Effat LK, El-Ruby MO.
    Genet Couns; 2012 Jun; 23(2):269-79. PubMed ID: 22876587
    [Abstract] [Full Text] [Related]

  • 37. RIPK4 promotes bladder urothelial carcinoma cell aggressiveness by upregulating VEGF-A through the NF-κB pathway.
    Liu JY, Zeng QH, Cao PG, Xie D, Chen X, Yang F, He LY, Dai YB, Li JJ, Liu XM, Zeng HL, Zhu YX, Gong L, Cheng Y, Zhou JD, Hu J, Bo H, Xu ZZ, Cao K.
    Br J Cancer; 2018 Jun; 118(12):1617-1627. PubMed ID: 29867225
    [Abstract] [Full Text] [Related]

  • 38. Alveolar synechia, ankyloblepharon, and ectodermal disorders: an autosomal recessive disorder?
    Ohishi M, Kai S, Ozeki S, Tashiro H.
    Am J Med Genet; 1991 Jan; 38(1):13-5. PubMed ID: 2012123
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  • 39. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant.
    Papadia F, Zimbalatti F, La Rosa CG.
    Am J Med Genet; 1984 Apr; 17(4):841-7. PubMed ID: 6720749
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  • 40. Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
    Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC.
    J Med Genet; 2003 Jun; 40(6):399-407. PubMed ID: 12807959
    [Abstract] [Full Text] [Related]

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