BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 17990920)

  • 1. Fraser syndrome: affected siblings born to nonconsanguineous parents and diagnosed at autopsy.
    De Jong A; Warren M; Rehrauer W; Harter J; Baraboo M; Chandra S; Pauli RM; Singer DB; Fritsch MK
    Pediatr Dev Pathol; 2008; 11(3):220-5. PubMed ID: 17990920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intrafamilial variability in Fraser syndrome.
    Prasun P; Pradhan M; Goel H
    Prenat Diagn; 2007 Aug; 27(8):778-82. PubMed ID: 17546704
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal death in Fraser syndrome.
    Comstock JM; Putnam AR; Opitz JM; Pysher TJ; Szakacs J
    Fetal Pediatr Pathol; 2005; 24(4-5):223-38. PubMed ID: 16396829
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs.
    Jadeja S; Smyth I; Pitera JE; Taylor MS; van Haelst M; Bentley E; McGregor L; Hopkins J; Chalepakis G; Philip N; Perez Aytes A; Watt FM; Darling SM; Jackson I; Woolf AS; Scambler PJ
    Nat Genet; 2005 May; 37(5):520-5. PubMed ID: 15838507
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Expressivity of familial forms of Fraser syndrome].
    Lambert JC; Touitou I; Paquis V; Saunières AM
    J Genet Hum; 1989 Jun; 37(2):119-26. PubMed ID: 2545810
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular study of 33 families with Fraser syndrome new data and mutation review.
    van Haelst MM; Maiburg M; Baujat G; Jadeja S; Monti E; Bland E; Pearce K; ; Hennekam RC; Scambler PJ
    Am J Med Genet A; 2008 Sep; 146A(17):2252-7. PubMed ID: 18671281
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks.
    Schauer GM; Dunn LK; Godmilow L; Eagle RC; Knisely AS
    Am J Med Genet; 1990 Dec; 37(4):583-91. PubMed ID: 2175543
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fraser syndrome: a new case report with review of the literature.
    Eskander BS; Shehata BM
    Fetal Pediatr Pathol; 2008; 27(2):99-104. PubMed ID: 18568997
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fraser Syndrome.
    Saleem AA; Siddiqui SN
    J Coll Physicians Surg Pak; 2015 Oct; 25 Suppl 2():S124-6. PubMed ID: 26522198
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects.
    Kiyozumi D; Sugimoto N; Sekiguchi K
    Proc Natl Acad Sci U S A; 2006 Aug; 103(32):11981-6. PubMed ID: 16880404
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recurrent Fraser syndrome.
    Kiran G; Namita G; Dheeraj S
    Prenat Diagn; 2007 Feb; 27(2):184-5. PubMed ID: 17266165
    [No Abstract]   [Full Text] [Related]  

  • 12. [Fraser syndrome: frequency in our environment and clinical-epidemiological aspects of a consecutive series of cases].
    Martínez-Frías ML; Bermejo Sánchez E; Félix V; Calvo Celada R; Ayala Garcés A; Hernández Ramón F
    An Esp Pediatr; 1998 Jun; 48(6):634-8. PubMed ID: 9662850
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.
    McGregor L; Makela V; Darling SM; Vrontou S; Chalepakis G; Roberts C; Smart N; Rutland P; Prescott N; Hopkins J; Bentley E; Shaw A; Roberts E; Mueller R; Jadeja S; Philip N; Nelson J; Francannet C; Perez-Aytes A; Megarbane A; Kerr B; Wainwright B; Woolf AS; Winter RM; Scambler PJ
    Nat Genet; 2003 Jun; 34(2):203-8. PubMed ID: 12766769
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fraser (Cryptophthalmos-syndactyly) syndrome: a case with bilateral anophthalmia but presence of normal eyelids.
    Pankau R; Partsch CJ; Jänig U; Meinecke R
    Genet Couns; 1994; 5(2):191-4. PubMed ID: 7917132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Fras1/Frem family of extracellular matrix proteins: structure, function, and association with Fraser syndrome and the mouse bleb phenotype.
    Petrou P; Makrygiannis AK; Chalepakis G
    Connect Tissue Res; 2008; 49(3):277-82. PubMed ID: 18661360
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome.
    Slavotinek A; Li C; Sherr EH; Chudley AE
    Am J Med Genet A; 2006 Sep; 140(18):1909-14. PubMed ID: 16894541
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variable presentation of Fraser syndrome in two fetuses and a novel mutation in FRAS1.
    Nayak SS; Salian S; Shukla A; Mathew M; Girisha KM
    Congenit Anom (Kyoto); 2017 May; 57(3):83-85. PubMed ID: 27624506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature.
    Berg C; Geipel A; Germer U; Pertersen-Hansen A; Koch-Dörfler M; Gembruch U
    Ultrasound Obstet Gynecol; 2001 Jul; 18(1):76-80. PubMed ID: 11489232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fraser syndrome.
    Kalpana Kumari MK; Kamath S; Mysorekar VV; Nandini G
    Indian J Pathol Microbiol; 2008; 51(2):228-9. PubMed ID: 18603689
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.
    Rousseau T; Laurent N; Thauvin-Robinet C; Lionnais S; Durand C; Faivre L; Sagot P
    Prenat Diagn; 2002 Aug; 22(8):692-6. PubMed ID: 12210578
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.