These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 25174843)

  • 1. Role of CGH array in the diagnosis of autosomal recessive disease: a case of Ellis-van Creveld syndrome.
    D'Ambrosio V; Votino C; Cos T; Boulanger S; Dheedene A; Jani J; Keymolen K
    Prenat Diagn; 2015 Jan; 35(1):97-9. PubMed ID: 25174843
    [No Abstract]   [Full Text] [Related]  

  • 2. [From gene to disease; EVC, EVC2, and Ellis-van Creveld syndrome].
    van Hagen JM; Baart JA; Gille JJ
    Ned Tijdschr Geneeskd; 2005 Apr; 149(17):929-31. PubMed ID: 15884406
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal Diagnosis of Ellis-van Creveld Syndrome by Targeted Sequencing.
    Hao XY; Fan CN; He YH; Liu JL; Ge SP
    Chin Med J (Engl); 2016 Aug; 129(15):1882-3. PubMed ID: 27453244
    [No Abstract]   [Full Text] [Related]  

  • 4. Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis.
    D'Asdia MC; Torrente I; Consoli F; Ferese R; Magliozzi M; Bernardini L; Guida V; Digilio MC; Marino B; Dallapiccola B; De Luca A
    Eur J Med Genet; 2013 Feb; 56(2):80-7. PubMed ID: 23220543
    [TBL] [Abstract][Full Text] [Related]  

  • 5. First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markers.
    Torrente I; Mangino M; De Luca A; Mingarelli R; Gennarelli M; Giannotti A; Novelli G; Dallapiccola B
    Prenat Diagn; 1998 May; 18(5):504-6. PubMed ID: 9621386
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ellis-van Creveld syndrome in adulthood: extending the clinical spectrum.
    Pérez-Andreu J; Ray VG; Arribas JM; Sánchez SJ
    Singapore Med J; 2015 Jun; 56(6):e110-1. PubMed ID: 26106249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling.
    Chen CP; Su YN; Hsu CY; Chern SR; Tsai FJ; Wu PC; Chen PT; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):481-6. PubMed ID: 21199751
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First trimester prenatal diagnosis of chondroectodermal dysplasia (Ellis-van Creveld syndrome) with ultrasound.
    Dugoff L; Thieme G; Hobbins JC
    Ultrasound Obstet Gynecol; 2001 Jan; 17(1):86-8. PubMed ID: 11244665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of chondroectodermal dysplasia (Ellis-van Creveld syndrome) with fetoscopy and ultrasound.
    Mahoney MJ; Hobbins JC
    N Engl J Med; 1977 Aug; 297(5):258-60. PubMed ID: 876300
    [No Abstract]   [Full Text] [Related]  

  • 10. Prenatal diagnosis of chondroectodermal dysplasia with fetoscopy.
    Bui TH; Marsk L; Eklöf O; Theorell K
    Prenat Diagn; 1984; 4(2):155-9. PubMed ID: 6739439
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ellis-van Creveld syndrome.
    Baujat G; Le Merrer M
    Orphanet J Rare Dis; 2007 Jun; 2():27. PubMed ID: 17547743
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Picture of the month. Ellis-van Creveld syndrome.
    Gellis SS; Feingold M
    Am J Dis Child; 1967 Aug; 114(2):169-70. PubMed ID: 4951541
    [No Abstract]   [Full Text] [Related]  

  • 13. [Ellis-van Creveld syndrome. Contribution of echography to prenatal diagnosis. Apropos of a case].
    Bérardi JC; Moulis M; Laloux V; Godard J; Wipff P; Botto C
    J Gynecol Obstet Biol Reprod (Paris); 1985; 14(1):43-7. PubMed ID: 3891835
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ellis-van Creveld syndrome in a fetus with rhizomelia and polydactyly. Report of a case diagnosed by genetic analysis, and correlation with pathological andradiologic findings.
    Peraita-Ezcurra M; Martínez-García M; Ruiz-Pérez VL; Sánchez-Gutiérrez ME; Fenollar-Cortés M; Vélez-Monsalve C; Ramos-Corrales C; Pastor I; Santonja C; Trujillo-Tiebas MJ
    Gene; 2012 May; 499(1):223-5. PubMed ID: 22406498
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome.
    Ruiz-Perez VL; Tompson SW; Blair HJ; Espinoza-Valdez C; Lapunzina P; Silva EO; Hamel B; Gibbs JL; Young ID; Wright MJ; Goodship JA
    Am J Hum Genet; 2003 Mar; 72(3):728-32. PubMed ID: 12571802
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Chondroectodermal dysplasia, Ellis-van Creveld syndrome].
    Masuno M
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):299-300. PubMed ID: 11057236
    [No Abstract]   [Full Text] [Related]  

  • 17. The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.
    Polymeropoulos MH; Ide SE; Wright M; Goodship J; Weissenbach J; Pyeritz RE; Da Silva EO; Ortiz De Luna RI; Francomano CA
    Genomics; 1996 Jul; 35(1):1-5. PubMed ID: 8661097
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Discordance for Ellis-van Creveld syndrome in twins.
    Thapa R; Mukhopadhyay M; Bhattacharya A
    Singapore Med J; 2008 Dec; 49(12):e369-71. PubMed ID: 19122938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome.
    Aziz A; Raza SI; Ali S; Ahmad W
    Clin Dysmorphol; 2016 Jan; 25(1):1-6. PubMed ID: 26580685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ellis van Creveld syndrome--a report of two siblings.
    Hegde K; Puthran RM; Nair G; Nair PP
    BMJ Case Rep; 2011 Oct; 2011():. PubMed ID: 22675019
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.