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Journal Abstract Search

281 related items for PubMed ID: 21978514

  • 1. [Adams-Oliver syndrome].
    Bayou F, Boussofara L, Bennani ZL, Ghariani N, Saïdi W, Belajouza C, Denguezli M, Nouira R.
    Ann Dermatol Venereol; 2011 Oct; 138(10):712-4. PubMed ID: 21978514
    [No Abstract] [Full Text] [Related]

  • 2. Adams-Oliver syndrome.
    Kutlubay Z, Pehlivan Ö.
    Int J Dermatol; 2014 Mar; 53(3):352-4. PubMed ID: 24320818
    [No Abstract] [Full Text] [Related]

  • 3. Adams Oliver Syndrome.
    Madan A, Sardana K, Garg VK.
    Indian Pediatr; 2015 Jul; 52(7):633-4. PubMed ID: 26244971
    [No Abstract] [Full Text] [Related]

  • 4. Adams-Oliver syndrome in a newborn infant.
    Zakanj Z, Bedek D, Kotrulja L, Ozanic Bulic S.
    Int J Dermatol; 2016 Feb; 55(2):215-7. PubMed ID: 24697559
    [No Abstract] [Full Text] [Related]

  • 5. [The Adams-Oliver syndrome. A case report].
    Yéo S, Perrot P, Bellier-Waast F, David A, Duteille F.
    Chir Main; 2010 Sep; 29(4):274-6. PubMed ID: 20727808
    [Abstract] [Full Text] [Related]

  • 6. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
    Yağci-Küpeli B, Çağlar K, Büyük S, Balci S.
    Genet Couns; 2011 Sep; 22(1):55-61. PubMed ID: 21614989
    [Abstract] [Full Text] [Related]

  • 7. Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.
    Vandersteen AM, Dixon JW.
    Clin Dysmorphol; 2011 Oct; 20(4):210-213. PubMed ID: 21785343
    [No Abstract] [Full Text] [Related]

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  • 9. Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.
    Jones KM, Silfvast-Kaiser A, Leake DR, Diaz LZ, Levy ML.
    Pediatr Dermatol; 2017 Sep; 34(5):e249-e253. PubMed ID: 28884918
    [Abstract] [Full Text] [Related]

  • 10. Adams-Oliver syndrome: new evidence in variable expressivity?
    Girish M, Mujawar N, Anekar U, Bhattad S.
    Int J Dermatol; 2014 Jul; 53(7):891-3. PubMed ID: 24372423
    [No Abstract] [Full Text] [Related]

  • 11. DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndrome.
    Aminkeng F.
    Clin Genet; 2015 Dec; 88(6):532. PubMed ID: 26419402
    [No Abstract] [Full Text] [Related]

  • 12. Adams-Oliver Syndrome - Follow-up of a Large Scalp Defect.
    Lorenz L, Sönnichsen K, Müller-Hansen I, Poets C.
    Klin Padiatr; 2014 Jul; 226(4):250-1. PubMed ID: 24515817
    [No Abstract] [Full Text] [Related]

  • 13. Adams-Oliver syndrome associated with gastrointestinal malformations.
    van Geyzel L, Gribbon C, Bradley S, Duffy D.
    BMJ Case Rep; 2016 Nov 25; 2016():. PubMed ID: 27888223
    [No Abstract] [Full Text] [Related]

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  • 17. Adams-Oliver Syndrome: Limited Expression.
    Kasinathan A, Sharawat IK, Das G, Sankhyan N.
    Indian J Pediatr; 2019 Jan 25; 86(1):101-102. PubMed ID: 29948730
    [No Abstract] [Full Text] [Related]

  • 18. Adams-Oliver syndrome: a case report.
    Frantz JA, Lehmkuhl RL, Leitis LH, Uliano VG, Siementcoski GA.
    Pediatr Dermatol; 2015 Jan 25; 32(3):383-5. PubMed ID: 25556654
    [Abstract] [Full Text] [Related]

  • 19. Mutations in NOTCH1 cause Adams-Oliver syndrome.
    Stittrich AB, Lehman A, Bodian DL, Ashworth J, Zong Z, Li H, Lam P, Khromykh A, Iyer RK, Vockley JG, Baveja R, Silva ES, Dixon J, Leon EL, Solomon BD, Glusman G, Niederhuber JE, Roach JC, Patel MS.
    Am J Hum Genet; 2014 Sep 04; 95(3):275-84. PubMed ID: 25132448
    [Abstract] [Full Text] [Related]

  • 20. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies.
    Sukalo M, Tilsen F, Kayserili H, Müller D, Tüysüz B, Ruddy DM, Wakeling E, Ørstavik KH, Snape KM, Trembath R, De Smedt M, van der Aa N, Skalej M, Mundlos S, Wuyts W, Southgate L, Zenker M.
    Hum Mutat; 2015 Jun 04; 36(6):593-8. PubMed ID: 25824905
    [Abstract] [Full Text] [Related]

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