Genetic studies in autistic disorders;Badania genetyczne w autyzmie dzieciȩcym

Psychiatria Polska

Volumn 34, Issue 3, 2000, Pages 435-446

  Slopien A ^a   Rajewski, A ^a  

^a Klin Psychiatr Dzieci i Mlodziezy   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 7; CHROMOSOME ABERRATION; GENETIC ANALYSIS; GILLES DE LA TOURETTE SYNDROME; MONOZYGOTIC TWINS; PATHOGENESIS; REVIEW; SEX DIFFERENCE; SIBLING; TUBEROUS SCLEROSIS; ULTRASTRUCTURE; CHILD; GENETICS; HUMAN; INFANT; PRESCHOOL CHILD; X CHROMOSOME;

AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; HUMANS; INFANT; X CHROMOSOME;

EID: 0034483759     PISSN: 00332674     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (57)

1. Asperger syndrome in a boy with a balanced de novo translocation: t(17;19)(p13.3;p11)
2. Hypomelanosis of Ito in three cases with autism and autistic-like conditions
3. Biochemiczne aspekty autyzmu - Implikacje praktyczne
4. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion
5. Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy
6. Demonstration of abnormal cyclic AMP production in platelets from patients with fragile X syndrome
7. Association of tuberous sclerosis of temporal lobes with autism and atypical autism
8. Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1)
9. Clinical and genetic relationships between autism-pervasive developmental disorder and Tourette syndrome: A study of 19 cases
10. Autism: Review of neurochemical investigation
11. Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder
12. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
13. Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3)
14. Is autism associated with the fragile X syndrome?
15. Autism and ring chromosome 18 mosaicism
16. Autism in Down's syndrome: Family history correlates
17. Autism and medical disorders: A review of the literature
18. Hypothyroidism and autism spectrum disorders
19. Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing
20. Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome
21. Executive function in parents of children with autism
22. A full genome screen for autism with evidence for linkage to a region on chromosome 7q
23. Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia
24. Molecular genetic analysis of the FMR-1 gene in a lange collection of autistic patients
25. Serotonin transporter (5-HTT) gene variants associated with autism?
26. A broader phenotype of autism: The clinical spectrum in twins
27. Polymorphism of FXR1 showing lack of association with autism
28. Intersitial deletion of 20p: New candidate region for Hirschsprung disease and autism?
29. No evidence of partial trisomy 16p in an autistic calendar savant with Torette syndrome
30. Gangliosides in cerebrospinal fluid in children with autism spectrum disorders
31. Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families
32. Personality and language characteristics in parents from multiple-incidence autism families
33. Biochemistry and psychophysiology of autistic syndromes
34. Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children
35. Genetic and child psychiatry: II empirical research findings
36. Autism and maternally derived aberrations of chromosome 15q
37. A clinical and molecular study of mosaicism for trisomy 17
38. Autism, affective disorders, and social phobia
39. Autism in Angelman Syndrome: A population-based study
40. Tics associated with autistic and pervasive developmental disorders
41. A mutation in adenylosuccinate lyase associated with mental retardation and autistic features
42. Tourette syndrome and autistic disorder: A significant relationship
43. Mutation screening of the UBE3A/E6-AP gene in autistic disorder
44. Case reports of autism with interstitial deletion of chromosome 17 (p11.2p11.2) and monosomy of chromosome 5 (5pter > 5p15.3)
45. Immunoglobulin A deficiency in a subset of autistic subjects
46. Strong association of the third hypervariable region of HLA-DR beta I with autism
47. CD4+ helper T cell depression in autism