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PUBMED FOR HANDHELDS

Journal Abstract Search


93 related items for PubMed ID: 23264967

  • 21. 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]

  • 22. The recognition of bilateral craniofacial deformities.
    Glass D.
    Trans Br Soc Study Orthod; 2014 Jul; 5(6):105-16. PubMed ID: 5290221
    [No Abstract] [Full Text] [Related]

  • 23. [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]

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

  • 25. 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
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  • 29. [Yunis-Varon syndrome].
    Nagai T.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb; (34 Pt 2):839-40. PubMed ID: 11529050
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  • 30. [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
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  • 31. Rescue of neurodegeneration in the Fig4 null mouse by a catalytically inactive FIG4 transgene.
    Lenk GM, Frei CM, Miller AC, Wallen RC, Mironova YA, Giger RJ, Meisler MH.
    Hum Mol Genet; 2016 Jan 15; 25(2):340-7. PubMed ID: 26604144
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  • 33. Cutis marmorata telangiectatica congenita.
    Garzon MC, Schweiger E.
    Semin Cutan Med Surg; 2004 Jun 15; 23(2):99-106. PubMed ID: 15295919
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  • 36. Ectrodactary, ectodermal dysplasia, and cleft lip-palate syndrome.
    Choong YY, Norazlina B.
    Med J Malaysia; 2001 Mar 15; 56(1):88-91. PubMed ID: 11503303
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  • 37. [The Adams-Oliver syndrome in Spain: the epidemiological aspects].
    Martínez-Frías ML, Arroyo Carrera I, Muñoz-Delgado NJ, Nieto Conde C, Rodríguez-Pinilla E, Urioste Azcorra M, Omeñaca Teres F, García Alix A.
    An Esp Pediatr; 1996 Jul 15; 45(1):57-61. PubMed ID: 8849132
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  • 40. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting.
    Pozo G, Canún S, Kofman-Alfaro S, Zenteno JC.
    Br J Dermatol; 2004 Oct 15; 151(4):930-2. PubMed ID: 15491445
    [No Abstract] [Full Text] [Related]


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