220 related articles for article (PubMed ID: 18261020)
1. Facial expression of affect in children with Cornelia de Lange syndrome.
Collis L; Moss J; Jutley J; Cornish K; Oliver C
J Intellect Disabil Res; 2008 Mar; 52(Pt 3):207-15. PubMed ID: 18261020
[TBL] [Abstract][Full Text] [Related]
2. Health and sleep problems in Cornelia de Lange Syndrome: a case control study.
Hall SS; Arron K; Sloneem J; Oliver C
J Intellect Disabil Res; 2008 May; 52(Pt 5):458-68. PubMed ID: 18341525
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Psychological well-being in parents of children with Angelman, Cornelia de Lange and Cri du Chat syndromes.
Griffith GM; Hastings RP; Oliver C; Howlin P; Moss J; Petty J; Tunnicliffe P
J Intellect Disabil Res; 2011 Apr; 55(4):397-410. PubMed ID: 21323782
[TBL] [Abstract][Full Text] [Related]
6. Simultaneous analysis of the behavioural phenotype, physical factors, and parenting stress in people with Cornelia de Lange syndrome.
Wulffaert J; van Berckelaer-Onnes I; Kroonenberg P; Scholte E; Bhuiyan Z; Hennekam R
J Intellect Disabil Res; 2009 Jul; 53(7):604-19. PubMed ID: 19522789
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes.
Moss JF; Oliver C; Berg K; Kaur G; Jephcott L; Cornish K
Am J Ment Retard; 2008 Jul; 113(4):278-91. PubMed ID: 18564888
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Clinical and genetic analysis of Korean patients with Cornelia de Lange syndrome: two novel NIPBL mutations.
Park HD; Ki CS; Kim JW; Kim WT; Kim JK
Ann Clin Lab Sci; 2010; 40(1):20-5. PubMed ID: 20124326
[TBL] [Abstract][Full Text] [Related]
10. Coeliac disease and Cornelia de Lange syndrome: lack of association.
Macchini F; Selicorni A; Luzzani S; Milani D; Roggero P; Valadè A
Acta Paediatr; 2007 Oct; 96(10):1518-20. PubMed ID: 17850398
[TBL] [Abstract][Full Text] [Related]
11. The behavioural phenotype of Cornelia de Lange Syndrome: a study of 56 individuals.
Basile E; Villa L; Selicorni A; Molteni M
J Intellect Disabil Res; 2007 Sep; 51(Pt 9):671-81. PubMed ID: 17845236
[TBL] [Abstract][Full Text] [Related]
12. Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation.
Selicorni A; Russo S; Gervasini C; Castronovo P; Milani D; Cavalleri F; Bentivegna A; Masciadri M; Domi A; Divizia MT; Sforzini C; Tarantino E; Memo L; Scarano G; Larizza L
Clin Genet; 2007 Aug; 72(2):98-108. PubMed ID: 17661813
[TBL] [Abstract][Full Text] [Related]
13. Incidence and clinical features of X-linked Cornelia de Lange syndrome due to SMC1L1 mutations.
Borck G; Zarhrate M; Bonnefont JP; Munnich A; Cormier-Daire V; Colleaux L
Hum Mutat; 2007 Feb; 28(2):205-6. PubMed ID: 17221863
[TBL] [Abstract][Full Text] [Related]
14. Characteristics of autism spectrum disorder in Cornelia de Lange syndrome.
Moss J; Howlin P; Magiati I; Oliver C
J Child Psychol Psychiatry; 2012 Aug; 53(8):883-91. PubMed ID: 22490014
[TBL] [Abstract][Full Text] [Related]
15. Father-to-daughter transmission of Cornelia de Lange syndrome caused by a mutation in the 5' untranslated region of the NIPBL Gene.
Borck G; Zarhrate M; Cluzeau C; Bal E; Bonnefont JP; Munnich A; Cormier-Daire V; Colleaux L
Hum Mutat; 2006 Aug; 27(8):731-5. PubMed ID: 16799922
[TBL] [Abstract][Full Text] [Related]
16. Social behavior and characteristics of autism spectrum disorder in Angelman, Cornelia de Lange, and Cri du Chat syndromes.
Moss J; Howlin P; Hastings RP; Beaumont S; Griffith GM; Petty J; Tunnicliffe P; Yates R; Villa D; Oliver C
Am J Intellect Dev Disabil; 2013 Jul; 118(4):262-83. PubMed ID: 23937369
[TBL] [Abstract][Full Text] [Related]
17. Survey of speech and language skills with prognostic indicators in 116 patients with Cornelia de Lange syndrome.
Goodban MT
Am J Med Genet; 1993 Nov; 47(7):1059-63. PubMed ID: 8291523
[TBL] [Abstract][Full Text] [Related]
18. Cornelia de Lange syndrome (CdLS): prenatal and autopsy findings.
Chong K; Keating S; Hurst S; Summers A; Berger H; Seaward G; Martin N; Friedberg T; Chitayat D
Prenat Diagn; 2009 May; 29(5):489-94. PubMed ID: 19242925
[TBL] [Abstract][Full Text] [Related]
19. Association between fatigue and autistic symptoms in children with cri du chat syndrome.
Claro A; Cornish K; Gruber R
Am J Intellect Dev Disabil; 2011 Jul; 116(4):278-89. PubMed ID: 21740256
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]