共 164 条
[1]
Bailey A. J.(1995)Autism as a strongly genetic disorder: Evidence from a British twin study Psychological Medicine 25 63-77
[2]
LeCouteur A.(1998)Duplication of 8p23.1: A cytogenetic anomaly with no established significance Journal of Medical Genetics 35 491-496
[3]
Gottesman A. A.(1990)Partial monosomy 8p with minimal dysmorphic signs Journal of Medical Genetics 27 327-329
[4]
Bolton P.(1994)A case-control family history study of autism Journal of Child Psychology and Psychiatry 35 877-900
[5]
Simonoff E.(1985)A case of autism and mosaic of trisomy 8 Journal of Autism and Developmental Disorders 15 351-352
[6]
Rutter M.(2001)Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity American Journal of Human Genetics 68 1514-1520
[7]
Barber J. C. K.(1997)A recognizable behavior phenotype associated with terminal deletions of the short arm of chromosome 8 American Journal of Medical Genetics 74 515-520
[8]
Joyce C. A.(1999)An autosomal genomic screen for autism American Journal of Medical Genetics 88 609-615
[9]
Collinson M. N.(1995)Inversion duplication of the short arm of chromosome 8: Clinical data on seven patients and review of the literature American Journal of Clinical Genetics 59 369-374
[10]
Nicholson M. N.(1999)Delineation of the critical region for congenital heart defects on chromosome 8p23.1 American Journal of Human Genetics 64 1119-1126