S D Smith

发表

Spelling errors in adults with a form of familial dyslexia.

H A Lubs, B. Pennington, H. Lubs, 1986, Child development.

Quantitative trait locus for reading disability: correction.

D W Fulker, L R Cardon, L. Cardon, 1995, Science.

Genetic influences on learning disabilities and speech and language disorders.

B. Pennington, S. Smith, B F Pennington, 1983, Child development.

Quantitative trait locus for reading disability on chromosome 6.

D W Fulker, L R Cardon, L. Cardon, 1994, Science.

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

C. Francks, S. Fisher, S. Vernes, 2017, Molecular Psychiatry.

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

G Van Camp, P Van de Heyning, C. Cremers, 1999, Human molecular genetics.

Molecular approaches to the genetic analysis of specific reading disability.

Shelley D. Smith, S. Smith, A. Brower, 1998, Human biology.

Evidence for linkage and association with reading disability on 6p21.3-22.

D E Kaplan, B. Pennington, Frank Wood, 2002, American journal of human genetics.

Etiology of Reading Difficulties and Rapid Naming: The Colorado Twin Study of Reading Disability

L R Cardon, L. Cardon, B. Pennington, 2001, Behavior genetics.

Genome-wide screening for DNA variants associated with reading and language traits

Timothy C. Bates, C. Francks, B. Pennington, 2014, Genes, brain, and behavior.