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 *

110 related articles for article (PubMed ID: 27145433)

  • 1. Benefits and limitations of a multidisciplinary approach to individualized management of Cornelia de Lange syndrome and related diagnoses.
    January K; Conway LJ; Deardorff M; Harrington A; Krantz ID; Loomes K; Pipan M; Noon SE
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):237-45. PubMed ID: 27145433
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Attitudes about the use of internet support groups and the impact among parents of children with Cornelia de Lange syndrome.
    Cacioppo CN; Conway LJ; Mehta D; Krantz ID; Noon SE
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):229-36. PubMed ID: 27163126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improvement in hearing loss over time in Cornelia de Lange syndrome.
    Janek KC; Smith DF; Kline AD; Benke JR; Chen ML; Kimball A; Ishman SL
    Int J Pediatr Otorhinolaryngol; 2016 Aug; 87():203-7. PubMed ID: 27368472
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sleep disorders in Cornelia de Lange syndrome.
    Zambrelli E; Fossati C; Turner K; Taiana M; Vignoli A; Gervasini C; Russo S; Furia F; Masciadri M; Ajmone P; Kullman G; Canevini MP; Selicorni A
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):214-21. PubMed ID: 27133889
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Contrasting age related changes in autism spectrum disorder phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up.
    Cochran L; Moss J; Nelson L; Oliver C
    Am J Med Genet C Semin Med Genet; 2015 Jun; 169(2):188-97. PubMed ID: 25989416
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cornelia de Lange syndrome: What every otolaryngologist should know.
    Eliason MJ; Melzer JM; Gallagher TQ
    Ear Nose Throat J; 2017 Aug; 96(8):E6-E9. PubMed ID: 28846791
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cornelia de Lange syndrome: a case study.
    Benson M
    Neonatal Netw; 2002 Apr; 21(3):7-13. PubMed ID: 12943206
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Causal explanations, concern and optimism regarding self-injurious behaviour displayed by individuals with Cornelia de Lange syndrome: the parents' perspective.
    Hyman P; Oliver C
    J Intellect Disabil Res; 2001 Aug; 45(Pt 4):326-34. PubMed ID: 11489054
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.
    Roshan Lal TR; Kliewer MA; Lopes T; Rebsamen SL; O'Connor J; Grados MA; Kimball A; Clemens J; Kline AD
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):190-7. PubMed ID: 27164360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case.
    Minor A; Shinawi M; Hogue JS; Vineyard M; Hamlin DR; Tan C; Donato K; Wysinger L; Botes S; Das S; Del Gaudio D
    Gene; 2014 Mar; 537(2):279-84. PubMed ID: 24378232
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interdisciplinary therapy in Cornelia de Lange syndrome - review of the literature.
    Mikołajewska E
    Adv Clin Exp Med; 2013; 22(4):571-7. PubMed ID: 23986218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cornelia de Lange syndrome and the Cohesin complex: Abstracts from the 9th Biennial Scientific and Educational Virtual Symposium 2020.
    Oliver C; Groves L; Hansen BD; Salehi M; Kheradmand S; Carrico CS; Caudill P; Mattingly M; Dorsett D; Chea S; Singh VP; Krantz ID; Huisman S; Deardorff MA; Kline AD
    Am J Med Genet A; 2022 Mar; 188(3):1005-1014. PubMed ID: 34877788
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome.
    Nakanishi M; Deardorff MA; Clark D; Levy SE; Krantz I; Pipan M
    Am J Med Genet A; 2012 Aug; 158A(8):1841-7. PubMed ID: 22740374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Challenges of caring for a patient with a rare disease--as demonstrated by Cornelia de Lange Syndrome.
    Wierzba J; Mazurkiewicz-Bełdzińska M; Jabłońska-Brudło J; Potaż P; Banach P
    Dev Period Med; 2015; 19(4):511-5. PubMed ID: 26982763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Special cases in Cornelia de Lange syndrome: The Spanish experience.
    Pié J; Puisac B; Hernández-Marcos M; Teresa-Rodrigo ME; Gil-Rodríguez M; Baquero-Montoya C; Ramos-Cáceres M; Bernal M; Ayerza-Casas A; Bueno I; Gómez-Puertas P; Ramos FJ
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):198-205. PubMed ID: 27164022
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A longitudinal follow-up study of affect in children and adults with Cornelia de Lange syndrome.
    Nelson L; Moss J; Oliver C
    Am J Intellect Dev Disabil; 2014 May; 119(3):235-52. PubMed ID: 24871792
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Natural history of aging in Cornelia de Lange syndrome.
    Kline AD; Grados M; Sponseller P; Levy HP; Blagowidow N; Schoedel C; Rampolla J; Clemens DK; Krantz I; Kimball A; Pichard C; Tuchman D
    Am J Med Genet C Semin Med Genet; 2007 Aug; 145C(3):248-60. PubMed ID: 17640042
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Advancing the Clinical and Molecular Understanding of Cornelia de Lange Syndrome: A Multidisciplinary Pediatric Case Series and Review of the Literature.
    Gruca-Stryjak K; Doda-Nowak E; Dzierla J; Wróbel K; Szymankiewicz-Bręborowicz M; Mazela J
    J Clin Med; 2024 Apr; 13(8):. PubMed ID: 38673696
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of limb differences in children with Cornelia de Lange Syndrome.
    Mehta D; Vergano SA; Deardorff M; Aggarwal S; Barot A; Johnson DM; Miller NF; Noon SE; Kaur M; Jackson L; Krantz ID
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):155-62. PubMed ID: 27120260
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome.
    Kawauchi S; Santos R; Muto A; Lopez-Burks ME; Schilling TF; Lander AD; Calof AL
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):138-45. PubMed ID: 27120001
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.