683 related articles for article (PubMed ID: 21790824)
41. [Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype].
Blanco-Barca O; Gallego-Blanco M; Ruiz-Ponte C; Barros-Angueira F; Esquete-López C; Eirís-Puñal J; Castro-Gago M
Rev Neurol; 2004 Jun 1-15; 38(11):1038-42. PubMed ID: 15202082
[TBL] [Abstract][Full Text] [Related]
42. Phenotype and natural history in Marshall-Smith syndrome.
Shaw AC; van Balkom ID; Bauer M; Cole TR; Delrue MA; Van Haeringen A; Holmberg E; Knight SJ; Mortier G; Nampoothiri S; Pušeljić S; Zenker M; Cormier-Daire V; Hennekam RC
Am J Med Genet A; 2010 Nov; 152A(11):2714-26. PubMed ID: 20949508
[TBL] [Abstract][Full Text] [Related]
43. Evidence for a discrete behavioral phenotype in the oculocerebrorenal syndrome of Lowe.
Kenworthy L; Charnas L
Am J Med Genet; 1995 Nov; 59(3):283-90. PubMed ID: 8599350
[TBL] [Abstract][Full Text] [Related]
44. [Autistic spectrum disorders in very young children: issues in the diagnostic process].
Sarimski K
Prax Kinderpsychol Kinderpsychiatr; 2006; 55(6):475-90. PubMed ID: 16967644
[TBL] [Abstract][Full Text] [Related]
45. A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms.
Zheng Z; Yao RE; Geng J; Jin X; Shen Y; Ying D; Fu Q; Yu Y
Gene; 2013 Mar; 516(2):301-6. PubMed ID: 23296059
[TBL] [Abstract][Full Text] [Related]
46. Fragile x syndrome and elimination disorders in a 6-year-old girl.
Equit M; Sambach H; von Gontard A
Klin Padiatr; 2011 Dec; 223(7):430-3. PubMed ID: 21563045
[TBL] [Abstract][Full Text] [Related]
47. Parenting children with and without developmental delay: the role of self-mastery.
Paczkowski E; Baker BL
J Intellect Disabil Res; 2007 Jun; 51(Pt. 6):435-46. PubMed ID: 17493027
[TBL] [Abstract][Full Text] [Related]
48. What symptoms predict the diagnosis of autism or PDD-NOS in infants and toddlers with developmental delays using the Baby and Infant Screen for aUtIsm Traits.
Matson JL; Fodstad JC; Dempsey T
Dev Neurorehabil; 2009; 12(6):381-8. PubMed ID: 20205546
[TBL] [Abstract][Full Text] [Related]
49. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
[No Abstract] [Full Text] [Related]
50. The behavioural phenotype of Smith-Magenis syndrome: evidence for a gene-environment interaction.
Taylor L; Oliver C
J Intellect Disabil Res; 2008 Oct; 52(10):830-41. PubMed ID: 18466291
[TBL] [Abstract][Full Text] [Related]
51. The structure of the Autism Diagnostic Interview-Revised: diagnostic and phenotypic implications.
Snow AV; Lecavalier L; Houts C
J Child Psychol Psychiatry; 2009 Jun; 50(6):734-42. PubMed ID: 19207624
[TBL] [Abstract][Full Text] [Related]
52. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.
Rogers SJ; Wehner DE; Hagerman R
J Dev Behav Pediatr; 2001 Dec; 22(6):409-17. PubMed ID: 11773805
[TBL] [Abstract][Full Text] [Related]
53. Social and communication behaviours in infants and toddlers with autism and pervasive developmental disorder-not otherwise specified.
Fodstad JC; Matson JL; Hess J; Neal D
Dev Neurorehabil; 2009 Jun; 12(3):152-7. PubMed ID: 19466623
[TBL] [Abstract][Full Text] [Related]
54. Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
Bay C; Mauk J; Radcliffe J; Kaplan P
Am J Med Genet; 1993 Nov; 47(7):965-8. PubMed ID: 7507294
[TBL] [Abstract][Full Text] [Related]
55. The validity of psychiatric diagnoses: the case of 'specific' developmental disorders.
Dyck MJ; Piek JP; Patrick J
Res Dev Disabil; 2011; 32(6):2704-13. PubMed ID: 21705192
[TBL] [Abstract][Full Text] [Related]
56. [Functioning of memory in subjects with autism].
Gras-Vincendon A; Bursztejn C; Danion JM
Encephale; 2008 Dec; 34(6):550-6. PubMed ID: 19081450
[TBL] [Abstract][Full Text] [Related]
57. Adaptive skills and executive function in autism spectrum disorders.
Gilotty L; Kenworthy L; Sirian L; Black DO; Wagner AE
Child Neuropsychol; 2002 Dec; 8(4):241-8. PubMed ID: 12759821
[TBL] [Abstract][Full Text] [Related]
58. Special report: aCGH for the genetic evaluation of patients with developmental delay/mental retardation or autism spectrum disorder.
Technol Eval Cent Assess Program Exec Summ; 2009 Apr; 23(10):1-5. PubMed ID: 19824216
[No Abstract] [Full Text] [Related]
59. Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome).
Sarasua SM; Dwivedi A; Boccuto L; Rollins JD; Chen CF; Rogers RC; Phelan K; DuPont BR; Collins JS
J Med Genet; 2011 Nov; 48(11):761-6. PubMed ID: 21984749
[TBL] [Abstract][Full Text] [Related]
60. Development of a test battery (NPM-X) for neuropsychological and neuromotor examination of children with developmental disabilities or mental retardation. A theoretical and clinical study.
Gjaerum B
Acta Psychiatr Scand Suppl; 1997; 390():1-55. PubMed ID: 9212855
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
