BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 27282200)

  • 21. Zimmermann-Laband syndrome in a patient with severe mental retardation.
    Van Buggenhout GJ; Brunner HG; Trommelen JC; Hamel BC
    Genet Couns; 1995; 6(4):321-7. PubMed ID: 8775419
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation in EED associated with overgrowth.
    Cohen AS; Tuysuz B; Shen Y; Bhalla SK; Jones SJ; Gibson WT
    J Hum Genet; 2015 Jun; 60(6):339-42. PubMed ID: 25787343
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome.
    Bakaeen G; Scully C
    J Oral Pathol Med; 1991 Oct; 20(9):457-9. PubMed ID: 1804991
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.
    Carvalho E; Honjo R; Magalhães M; Yamamoto G; Rocha K; Naslavsky M; Zatz M; Passos-Bueno MR; Kim C; Bertola D
    Am J Med Genet A; 2015 May; 167A(5):1039-46. PubMed ID: 25663181
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DOORS syndrome: phenotype, genotype and comparison with Coffin-Siris syndrome.
    Campeau PM; Hennekam RC;
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):327-32. PubMed ID: 25169651
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
    Abo-Dalo B; Kim HG; Roes M; Stefanova M; Higgins A; Shen Y; Mundlos S; Quade BJ; Gusella JF; Kutsche K
    Am J Med Genet A; 2007 Nov; 143A(22):2668-74. PubMed ID: 17937436
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations.
    Chadwick B; Hunter B; Hunter L; Aldred M; Wilkie A
    Oral Surg Oral Med Oral Pathol; 1994 Jul; 78(1):57-63. PubMed ID: 8078665
    [TBL] [Abstract][Full Text] [Related]  

  • 28. West syndrome in a patient with Schinzel-Giedion syndrome.
    Miyake F; Kuroda Y; Naruto T; Ohashi I; Takano K; Kurosawa K
    J Child Neurol; 2015 Jun; 30(7):932-6. PubMed ID: 25028416
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A case of Zimmermann-Laband syndrome with supernumerary teeth.
    Holzhausen M; Gonçalves D; Corrêa Fde O; Spolidorio LC; Rodrigues VC; Orrico SR
    J Periodontol; 2003 Aug; 74(8):1225-30. PubMed ID: 14514238
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The orthodontic and surgical management of Zimmerman-Laband syndrome.
    Perks T; Popat H; Cronin AJ; Durning P; Maggs R
    Orthodontics (Chic.); 2013; 14(1):e168-76. PubMed ID: 23646327
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Temple-Baraitser syndrome: a rare and possibly unrecognized condition.
    Jacquinet A; Gérard M; Gabbett MT; Rausin L; Misson JP; Menten B; Mortier G; Van Maldergem L; Verloes A; Debray FG
    Am J Med Genet A; 2010 Sep; 152A(9):2322-6. PubMed ID: 20683999
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
    Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
    [No Abstract]   [Full Text] [Related]  

  • 33. Cerebro-fronto-facial syndrome type 3 with polymicrogyria: a clinical presentation of Baraitser-Winter syndrome.
    Eker HK; Derinkuyu BE; Ünal S; Masliah-Planchon J; Drunat S; Verloes A
    Eur J Med Genet; 2014 Jan; 57(1):32-6. PubMed ID: 24211661
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Numerous BAF complex genes are mutated in Coffin-Siris syndrome.
    Miyake N; Tsurusaki Y; Matsumoto N
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):257-61. PubMed ID: 25081545
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Zimmermann-Laband syndrome with bilateral developmental cataract - a new association?
    Shah N; Gupta YK; Ghose S
    Int J Paediatr Dent; 2004 Jan; 14(1):78-85. PubMed ID: 14706033
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [The Zimmermann-Laband syndrome].
    Pfeiffer RA; Seemanova E; Süss J; Müssig D; Tietze HU
    Klin Padiatr; 1992; 204(1):1-5. PubMed ID: 1740896
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A further patient with van Maldergem syndrome.
    Neuhann TM; Müller D; Hackmann K; Holzinger S; Schrock E; Di Donato N
    Eur J Med Genet; 2012 Jun; 55(6-7):423-8. PubMed ID: 22469822
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fryns syndrome without diaphragmatic hernia, DOOR syndrome or Fryns-like syndrome? Report on patients from Indian Ocean islands.
    Alessandri JL; Cuillier F; Malan V; Brayer C; Grondard M; Jacquemot-Dekkak L; Kieffer-Traversier M; Pierre F; Laurain C; Samperiz S; Tiran-Rajaofera I; Ramful D
    Am J Med Genet A; 2014 Mar; 164A(3):648-54. PubMed ID: 24357154
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Applications of next-generation whole exome sequencing.
    Harding KE; Robertson NP
    J Neurol; 2014 Jun; 261(6):1244-6. PubMed ID: 24838538
    [No Abstract]   [Full Text] [Related]  

  • 40. Phenotype-genotype complexities: opening DOORS.
    Berkovic SF; Gecz J
    Lancet Neurol; 2014 Jan; 13(1):24-5. PubMed ID: 24291219
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.