Chromosomal abnormalities in a clinic sample of individuals with autistic disorder

Psychiatric Genetics

Volumn 11, Issue 2, 2001, Pages 57-63

  Wassink, Thomas H ^a,c   Piven, Joseph ^b   Patil, Shivanand R ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

Autism; Chromosomal abnormalities; Genetics; Karyotype; Mental retardation

Indexed keywords

ARTICLE; AUTISM; CHROMOSOME 15; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; DATA BASE; FEMALE; FRAGILE X SYNDROME; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; SEX CHROMOSOME ABERRATION;

ABNORMALITIES, MULTIPLE; AUTISTIC DISORDER; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; COMORBIDITY; EPILEPSY; FEMALE; FRAGILE X SYNDROME; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IOWA; KARYOTYPING; MALE; MENTAL RETARDATION; RETROSPECTIVE STUDIES; SEX CHROMOSOME DISORDERS;

EID: 0034944526     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041444-200106000-00001     Document Type: Article

References (64)

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. Genetic studies of autistic disorder and chromosome 7
3. Prevalence of the Fragile X anomaly amongst autistic twins and singletons
4. Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder
5. Autistic disorder associated with an iso-dicentric Y chromosome
6. Frequency of the Fragile X syndrome in infantile autism. A Swedish multicenter study
7. Association of Fragile X syndrome with autism
8. Autism is associated with the Fragile-X syndrome
9. Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia
10. An autosomal genomic screen for autism
11. Evidence of linkage between the serotonin transporter and autistic disorder
12. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
13. Prader - Willi syndrome
14. Three patients with a 45,X/46,X,psu dic(Xp) karyotype
15. Female with autistic disorder and monosomy X (Turner Syndrome): Parent-of-origin effect of the X chromosome
16. Autism: The point of view from Fragile X studies
17. The epidemiology of autism: A review
18. Prevalence of infantile autism in four French regions
19. Autism and associated medical disorders in a French epidemiological survey
20. Chromosomal disorders and autism
21. Chromosome abnormalities in infantile autism and other childhood psychoses: A population study of 66 cases
22. Infantile autism in children of immigrant parents. A population-based study from Goteborg, Sweden
23. Is autism more common now than ten years ago?
24. Autism associated with marker chromosome
25. Autism in Fragile X females
26. An analysis of autism in fifty males with the Fragile X syndrome
27. Autism and the X chromosome. Multipoint sib-pair analysis
28. The recognition of autism in children with Down syndrome - Implications for intervention and some speculations about pathology
29. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium
30. Search for autism susceptibility loci: Genome screen follow-up and fine mapping of a candidate region on chromosome 7q
31. Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3′ to the SDC2 gene
32. Comorbidity of autistic spectrum disorders in children with Down syndrome
33. Autism, profound mental retardation and atypical bipolar disorder in a 33-year-old female with a deletion of 15q12
34. Serotonin transporter (5-HTT) gene variants associated with autism?
35. Chromosomal abnormalities in a series of children with autistic disorder
36. Angelman syndrome: A review of clinical and genetic aspects
37. Infantile autism and associated autosomal chromosome abnormalities: A register-based study and a literature survey
38. Molecular and cytogenetic analyses of autism in Taiwan
39. Autism, mental retardation, and chromosomal abnormalities
40. 47,XYY karyotypes and pervasive developmental disorders
41. Epilepsy in autism and autisticlike conditions. A population-based study
42. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
43. The prevalence of Fragile X in a sample of autistic individuals diagnosed using a standardized interview
44. Molecular cytogenetic analysis of a duplication Xp in a male: Further delineation of a possible sex influencing region on the X chromosome
45. Autistic symptoms among children and young adults with isodicentric chromosome 15
46. A genomic screen of autism: Evidence for a multilocus etiology
47. The UCLA-University of Utah epidemiologic survey of autism: Prevalence
48. The UCLA-University of Utah epidemiologic survey of autism: The etiologic role of rare diseases
49. Chromosome 15q11-13 region and the autistic disorder
50. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism
51. Autistic disorder and additional inv dup(15)(pter-q13) chromosome
52. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
53. Autism and autistic-like conditions in Swedish rural and urban areas: A population study
54. Autism in Angelman syndrome: A population-based study
55. A community survey of infantile autism
56. Linkage analysis with adequate modeling of a parent-of-origin effect
57. Cloning of a candidate gene (ARG1) from the breakpoint of t(7;20) in an autistic twin pair
58. Xp deletions associated with autism in three females
59. Prevalence of fra(X) and other specific diagnoses in autistic individuals in a Danish county
60. Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual
61. Evidence supporting WNT2 as an autism susceptibility gene
62. Chromosomes in autism and related pervasive developmental disorders: A cytogenetic study
63. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
64. The prevalence of early childhood autism: Comparison of administrative and epidemiological studies