NotesFAQContact Us
Collection
Advanced
Search Tips
Showing all 7 results Save | Export
Peer reviewed Peer reviewed
Alarcon, Marciela; DeFries, John C.; Light, Jacquelyn Gillis; Pennington, Bruce F. – Journal of Learning Disabilities, 1997
Comparison of twins (40 identical and 23 fraternal) for mathematics deficits (MD), in which at least one member had a mathematics disability, found evidence for a significant genetic etiology. However, tests for the differential etiology of MD as a function of reading performance level were nonsignificant. (Author/DB)
Descriptors: Etiology, Genetics, Heredity, Incidence
Peer reviewed Peer reviewed
Mazzocco, Michele M. M. – Journal of Learning Disabilities, 2001
This study examined whether indicators of math learning disability were observed in 35 5- and 6-year-olds with either neurofibromatosis, Turner Syndrome, or fragile X syndrome and compared to controls. Findings indicate that girls with fragile X or Turner syndrome but not neurofibromatosis are significantly more likely to have specific math…
Descriptors: Congenital Impairments, Females, Genetics, Learning Disabilities
Peer reviewed Peer reviewed
Light, Jacquelyn Gillis; DeFries, John C. – Journal of Learning Disabilities, 1995
Data from 148 identical and 111 fraternal twin pairs in which at least 1 member had a reading disability were statistically analyzed. Results suggest that genetic and shared-environment influences both contribute to the observed covariance between reading and mathematical deficits. (Author/DB)
Descriptors: Etiology, Family Environment, Genetics, Learning Disabilities
Peer reviewed Peer reviewed
Smith, Sandra – Annals of Dyslexia, 1992
Pedigree analysis of 12 young adults (9 of whom had learning disabilities) indicated that learning disability (LD) was strongly familial but that the type of disability (reading or math) was not directly inherited. Autoimmune disorders were significantly correlated with LD. In seven of the LD families, adults failed to overcome earlier reading and…
Descriptors: Family Influence, Genetics, Heredity, Incidence
Peer reviewed Peer reviewed
Ozonoff, Sally; And Others – Journal of Autism and Developmental Disorders, 1993
This study provides support for a potential subclinical marker in the executive function domain of siblings (n=18, ages 8-18) of autistic individuals, compared to learning-disabled controls. No group differences in theory-of-mind abilities were found. The need to develop more sensitive measures is discussed. (Author/JDD)
Descriptors: Autism, Biological Influences, Cognitive Processes, Etiology
Peer reviewed Peer reviewed
Olson, Richard; And Others – Journal of Learning Disabilities, 1989
Word recognition data from identical and fraternal twins and siblings (N=172) indicated that the phonological coding deficit of children with reading disabilities was highly heritable. Orthographic coding was not significantly heritable. Poor readers with low IQs were superior to similar reading but average IQ readers in phonological coding.…
Descriptors: Elementary Secondary Education, Genetics, Heredity, Intelligence Differences
Peer reviewed Peer reviewed
Rovet, Joanne; And Others – Journal of Learning Disabilities, 1996
This article integrates the literature on intelligence and achievement outcomes in boys with Klinefelter syndrome (KS). It reports results of a study following 36 boys with KS and 33 sibling controls. Boys with KS demonstrated verbal cognitive deficits and significant underachievement in reading, spelling, and arithmetic, which increased with age.…
Descriptors: Academic Achievement, Age, Arithmetic, Cognitive Ability