The turner syndrome-associated neurocognitive phenotype maps to distal Xp

American Journal of Human Genetics

Volumn 67, Issue 3, 2000, Pages 672-681

  Ross, Judith L ^a   Roeltgen, David ^c   Kushner, Harvey ^b   Wei, Fanglin ^d   Zinn, Andrew R ^d  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

^b Biomedical Computer Research Institute   (United States)

^c PENN STATE COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME MAP; COGNITION; DEPTH PERCEPTION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC MARKER; GENETIC POLYMORPHISM; HETEROZYGOSITY; HUMAN; KARYOTYPING; PHENOTYPE; PRIORITY JOURNAL; STATISTICAL ANALYSIS; TRISOMY 21; TURNER SYNDROME; X CHROMOSOME;

EID: 0033846539     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303039     Document Type: Article

References (48)

1. Anthropometric craniofacial pattern profiles in Down syndrome
2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
3. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome
4. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
5. A cognitive development of unselected girls with complete and partial X monosomy
6. Evidence for a pseudo-autosomal locus for schizophrenia using the method of affected sibling pairs
7. A diphasic pattern of gonadotropin secretion in patients with the syndrome of gonadal dysgenesis
8. Sex chromosomes and psychosis: The case for a pseudoautosomal locus
9. Cognitive ability and everyday functioning in women with Turner syndrome
10. Mechanisms leading to the phenotype of Turner syndrome
11. The conceptual bases for the phenotypic mapping of conditions resulting from aneuploidy
12. LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition
13. Deletions of Xq and growth deficit: A review
14. A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere
15. Establishment of permanent cell lines by Epstein-Barr virus transformation
16. Learning disorders and sex chromosome aberrations
17. A study of females with deletions of the short arm of the X chromosome
18. Xp pseudoautosomal gene haploin-sufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation
19. Recognizing Ullrich-Turner syndrome by discriminant analysis of craniofacial structure
20. Expression cloning of the human IL-3 receptor cDNA reveals a shared beta subunit for the human IL-3 and GM-CSF receptors
21. Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: Implications for the development of Turner syndrome
22. IXDB, an X chromosome integrated database (update)
23. The Turner syndrome: Cognitive deficits, affective discrimination, and behavior problems
24. Visuospatial construction
25. Turner syndrome and parietal lobe functions
26. Atypical hemispheric lateralization in Turner syndrome subjects
27. The neuropsychological phenotype in Turner syndrome
28. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
29. Neurodevelopmental effects of X monosomy: A volumetric imaging study
30. Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: Isolation of the gene ASMTL
31. The transition to young-adulthood in Ullrich-Turner syndrome: Neurodevelopmental changes
32. Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile
33. Estrogen effects on nonverbal processing speed and motor function in girls with Turner syndrome
34. Use of estrogen in young girls with Turner syndrome: Effects on memory
35. Ullrich-Turner syndrome: Neurodevelopmental changes from childhood through adolescence
36. The cognitive and neuropsychological characteristics of females with Turner syndrome
37. A high resolution deletion map of human chromosome Xp22
38. A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation
39. Mutation and deletion of the pseudoautosomal gene SHOX cause LeriWeill dyschondrosteosis
40. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
41. Intelligence, behavior, and psychosocial development in Turner syndrome
42. Xp deletions associated with autism in three females
43. Mental retardation in Turner syndrome
44. Neuropsychological aspects of Turner syndrome
45. Localization of the hydroxyindole-O-methyltransferase gene to the pseudoautosomal region: Implications for mapping of psychiatric disorders
46. Turner syndrome: The case of the missing sex chromosome
47. Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1