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 *

129 related articles for article (PubMed ID: 20425817)

  • 1. Cornelia de Lange syndrome: extending the physical and psychological phenotype.
    Oliver C; Bedeschi MF; Blagowidow N; Carrico CS; Cereda A; Fitzpatrick DR; Gervasini C; Griffith GM; Kline AD; Marchisio P; Moss J; Ramos FJ; Selicorni A; Tunnicliffe P; Wierzba J; Hennekam RC
    Am J Med Genet A; 2010 May; 152A(5):1127-35. PubMed ID: 20425817
    [No Abstract]   [Full Text] [Related]  

  • 2. Chromatinopathies: A focus on Cornelia de Lange syndrome.
    Avagliano L; Parenti I; Grazioli P; Di Fede E; Parodi C; Mariani M; Kaiser FJ; Selicorni A; Gervasini C; Massa V
    Clin Genet; 2020 Jan; 97(1):3-11. PubMed ID: 31721174
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Behavioural phenotype of Cornelia de Lange syndrome: case-control study.
    Oliver C; Arron K; Sloneem J; Hall S
    Br J Psychiatry; 2008 Dec; 193(6):466-70. PubMed ID: 19043149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome.
    Hayashi M; Sakamoto K; Kurata K; Nagata J; Satoh J; Morimatsu Y
    Acta Neuropathol; 1996 Dec; 92(6):625-30. PubMed ID: 8960322
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL.
    Lalatta F; Russo S; Gentilin B; Spaccini L; Boschetto C; Cavalleri F; Masciadri M; Gervasini C; Bentivegna A; Castronovo P; Larizza L
    Genet Med; 2007 Mar; 9(3):188-94. PubMed ID: 17413424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Functional Mutation in HDAC8 Gene as Novel Diagnostic Marker for Cornelia De Lange Syndrome.
    Gao X; Huang Z; Fan Y; Sun Y; Liu H; Wang L; Gu XF; Yu Y
    Cell Physiol Biochem; 2018; 47(6):2388-2395. PubMed ID: 29991052
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Novel Frameshift Mutation (c.5387_5388insTT) in
    Kang MJ; Ahn SM; Hwang IT
    Ann Clin Lab Sci; 2018 Jan; 48(1):106-109. PubMed ID: 29531005
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Autopsy case of Cornelia de Lange syndrome with chromosome abnormalities].
    Kubota Y; Okada Y; Matsui I; Hayashi Y; Takazawa H
    Nihon Shonika Gakkai Zasshi; 1970 Jan; 74(1):1-9. PubMed ID: 5462021
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Omphalocele in an infant with Cornelia de Lange syndrome.
    Lemire EG
    Clin Dysmorphol; 2006 Oct; 15(4):255-256. PubMed ID: 16957487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes.
    Watkins A; Bissell S; Moss J; Oliver C; Clayton-Smith J; Haye L; Heald M; Welham A
    J Neurodev Disord; 2019 Oct; 11(1):24. PubMed ID: 31586495
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Cornelia de Lange syndrome. Presentation of a clinical case].
    Perri PF; Tubaldi L; Amadori O
    Pediatr Med Chir; 1987; 9(4):499-501. PubMed ID: 3697331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effects of social context on social interaction and self-injurious behavior in Cornelia de Lange syndrome.
    Arron K; Oliver C; Hall S; Sloneem J; Forman D; McClintock K
    Am J Ment Retard; 2006 May; 111(3):184-92. PubMed ID: 16597185
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype.
    Parenti I; Gervasini C; Pozojevic J; Graul-Neumann L; Azzollini J; Braunholz D; Watrin E; Wendt KS; Cereda A; Cittaro D; Gillessen-Kaesbach G; Lazarevic D; Mariani M; Russo S; Werner R; Krawitz P; Larizza L; Selicorni A; Kaiser FJ
    Clin Genet; 2016 Jan; 89(1):74-81. PubMed ID: 25652421
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cornelia de Lange Syndrome and multiple hormonal deficiency, an unusual association. Clinical case].
    Mora-Bautista VM; Mendoza-Rojas V; Contreras-García GA
    Arch Argent Pediatr; 2017 Jun; 115(3):e170-e174. PubMed ID: 28504504
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dental findings in Cornelia de Lange syndrome.
    Toker AS; Ay S; Yeler H; Sezgin I
    Yonsei Med J; 2009 Apr; 50(2):289-92. PubMed ID: 19430566
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cornelia de Lange syndrome--photo essay.
    Ireland M; Burn J
    Clin Dysmorphol; 1993 Apr; 2(2):151-60. PubMed ID: 8281279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.
    Avagliano L; Grazioli P; Mariani M; Bulfamante GP; Selicorni A; Massa V
    Orphanet J Rare Dis; 2017 Nov; 12(1):174. PubMed ID: 29162129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review.
    Liu C; Li X; Cui J; Dong R; Lv Y; Wang D; Zhang H; Li X; Li Z; Ma J; Liu Y; Gai Z
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1471. PubMed ID: 32856424
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Repetitive and Self-injurious Behaviors in Children with Cornelia de Lange Syndrome.
    Srivastava S; Clark B; Landy-Schmitt C; Offermann EA; Kline AD; Wilkinson ST; Grados MA
    J Autism Dev Disord; 2021 May; 51(5):1748-1758. PubMed ID: 32809170
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.