BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

470 related articles for article (PubMed ID: 15844775)

  • 1. A de novo t (X;8)(p11.2;q24.3) demonstrating Cornelia de Lange syndrome phenotype.
    Egemen A; Ulger Z; Ozkinay F; Gulen F; Cogulu O
    Genet Couns; 2005; 16(1):27-30. PubMed ID: 15844775
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome 13q deletion with Cornelia de Lange syndrome phenotype.
    Ngo CT; Alhady M; Tan AK; Norlasiah IS; Ong GB; Chua CN
    Med J Malaysia; 2007 Mar; 62(1):74-5. PubMed ID: 17682579
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy.
    Chen CP; Lin SP; Liu YP; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Wang W
    Gene; 2013 Oct; 529(1):176-80. PubMed ID: 23933416
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.
    Dundar M; Uzak A; Erdogan M; Saatci C; Akdeniz S; Luleci G; Keser I; Karauzum S
    Genet Couns; 2011; 22(2):199-205. PubMed ID: 21848013
    [TBL] [Abstract][Full Text] [Related]  

  • 5. NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
    Borck G; Redon R; Sanlaville D; Rio M; Prieur M; Lyonnet S; Vekemans M; Carter NP; Munnich A; Colleaux L; Cormier-Daire V
    J Med Genet; 2004 Dec; 41(12):e128. PubMed ID: 15591270
    [No Abstract]   [Full Text] [Related]  

  • 6. Double outlet right ventricle and aortopulmonary window in a patient with Cornelia de Lange syndrome: a novel association.
    Akdeniz C; Odemis E; Erdem A; Celebi A
    Genet Couns; 2009; 20(2):161-6. PubMed ID: 19650413
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients.
    Schoumans J; Wincent J; Barbaro M; Djureinovic T; Maguire P; Forsberg L; Staaf J; Thuresson AC; Borg A; Nordgren A; Malm G; Anderlid BM
    Eur J Hum Genet; 2007 Feb; 15(2):143-9. PubMed ID: 17106445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomes in the Cornelia de Lange syndrome.
    Beck B; Mikkelsen M
    Hum Genet; 1981; 59(4):271-6. PubMed ID: 7333580
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings.
    Bhuiyan ZA; Zilfalil BA; Hennekam RC
    Singapore Med J; 2006 Aug; 47(8):724-7. PubMed ID: 16865217
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.
    Ireland M; English C; Cross I; Houlsby WT; Burn J
    J Med Genet; 1991 Sep; 28(9):639-40. PubMed ID: 1956066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndrome.
    Baynam G; Goldblatt J; Walpole I
    Am J Med Genet A; 2008 Jun; 146A(12):1565-70. PubMed ID: 18470924
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cornelia de Lange syndrome in an Egyptian child.
    Temtamy SA; Shoukry AS
    Birth Defects Orig Artic Ser; 1975; 11(2):362-3. PubMed ID: 1227551
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cornelia de Lange syndrome: evolution of the phenotype.
    Passarge E; Mecke S; Altrogge HC
    Pediatrics; 1971 Nov; 48(5):833-6. PubMed ID: 5121247
    [No Abstract]   [Full Text] [Related]  

  • 14. [Brachmann-de Lange syndrome in 16 of our patients].
    Pankau R; Johannson W; Meinecke P
    Monatsschr Kinderheilkd; 1990 Feb; 138(2):72-6. PubMed ID: 2320015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal anomaly associated with Cornelia de Lange's syndrome.
    Szemere G; Godó B; Osváth P; Lehrner J; Pataki O
    Acta Paediatr Acad Sci Hung; 1972; 13(1):51-5. PubMed ID: 4652495
    [No Abstract]   [Full Text] [Related]  

  • 16. Cornelia de Lange syndrome associated with a de-novo novel NIPBL splice-site mutation and a coincidental inherited translocation t(3;5)(p13;q11).
    Wierzba J; Kuzniacka A; Ratajska M; Lipska BS; Kardas I; Iliszko M; Limon J
    Clin Dysmorphol; 2011 Oct; 20(4):222-224. PubMed ID: 21666440
    [No Abstract]   [Full Text] [Related]  

  • 17. Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21).
    Witters I; Balikova I; Cannie M; Devriendt K; De Catte L; Fryns JP
    Genet Couns; 2008; 19(4):443-6. PubMed ID: 19239091
    [No Abstract]   [Full Text] [Related]  

  • 18. [Systemic and ophthalmological findings in Cornelia de Lange syndrome].
    Mrugacz M; Sielicka D
    Klin Oczna; 2012; 114(1):68-70. PubMed ID: 22783750
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Chromosome abnormalities in a case of Cornelia De Lange syndrome (typus degenerativus amstedolamensis)].
    de Angelis P; Ventruto V
    Minerva Pediatr; 1976 Mar; 28(7):449-53. PubMed ID: 1004448
    [No Abstract]   [Full Text] [Related]  

  • 20. [Similarity between the syndrome of partial trisomy of the long arm of chromosome 3 and the Cornelia de Lange syndrome].
    Polívková Z; Kucerová M; Dolanská M; Hresová M; Kofer J
    Cesk Pediatr; 1988 Dec; 43(12):723-6. PubMed ID: 3250742
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 24.