Kimberling WJ - Search Results

1

Familial dyslexia: use of genetic linkage data to define subtypes.

Smith SD, Pennington BF, Kimberling WJ, Ing PS. Smith SD, et al. Among authors: kimberling wj. J Am Acad Child Adolesc Psychiatry. 1990 Mar;29(2):204-13. doi: 10.1097/00004583-199003000-00008. J Am Acad Child Adolesc Psychiatry. 1990. PMID: 1969860

2

Dyslexia subtypes: genetics, behavior, and brain imaging.

Lubs HA, Smith S, Kimberling W, Pennington B, Gross-Glenn K, Duara R. Lubs HA, et al. Res Publ Assoc Res Nerv Ment Dis. 1988;66:139-47. Res Publ Assoc Res Nerv Ment Dis. 1988. PMID: 3258668

3

Specific reading disability: identification of an inherited form through linkage analysis.

Smith SD, Kimberling WJ, Pennington BF, Lubs HA. Smith SD, et al. Among authors: kimberling wj. Science. 1983 Mar 18;219(4590):1345-7. doi: 10.1126/science.6828864. Science. 1983. PMID: 6828864

4

Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.

Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW. Kumar S, et al. Among authors: kimberling wj. Genomics. 1996 Jan 1;31(1):71-9. doi: 10.1006/geno.1996.0011. Genomics. 1996. PMID: 8808282 Free article.

5

National Deaf Register as a resource for hereditary deafness research.

Ing PS, Wernimont BM, Smith SD, Kimberling WJ. Ing PS, et al. Among authors: kimberling wj. Ann N Y Acad Sci. 1991;630:292. doi: 10.1111/j.1749-6632.1991.tb19609.x. Ann N Y Acad Sci. 1991. PMID: 1952610 No abstract available.

6

Spelling errors in adults with a form of familial dyslexia.

Pennington BF, McCabe LL, Smith SD, Lefly DL, Bookman MO, Kimberling WJ, Lubs HA. Pennington BF, et al. Among authors: kimberling wj. Child Dev. 1986 Aug;57(4):1001-13. doi: 10.1111/j.1467-8624.1986.tb00261.x. Child Dev. 1986. PMID: 3757596

7

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Kimberling WJ, Weston MD, Möller C, van Aarem A, Cremers CW, Sumegi J, Ing PS, Connolly C, Martini A, Milani M, et al. Kimberling WJ, et al. Am J Hum Genet. 1995 Jan;56(1):216-23. Am J Hum Genet. 1995. PMID: 7825581 Free PMC article.

8

Medical genetic evaluation for the etiology of hearing loss in children.

Smith SD, Kimberling WJ, Schaefer GB, Horton MB, Tinley ST. Smith SD, et al. Among authors: kimberling wj. J Commun Disord. 1998 Sep-Oct;31(5):371-88; quiz 388-9. doi: 10.1016/s0021-9924(98)00011-2. J Commun Disord. 1998. PMID: 9777485 Review.

9

Left-handedness and immune disorders in familial dyslexics.

Pennington BF, Smith SD, Kimberling WJ, Green PA, Haith MM. Pennington BF, et al. Among authors: kimberling wj. Arch Neurol. 1987 Jun;44(6):634-9. doi: 10.1001/archneur.1987.00520180054016. Arch Neurol. 1987. PMID: 3579681

10

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Am J Hum Genet. 1998 Apr;62(4):792-9. doi: 10.1086/301807. Am J Hum Genet. 1998. PMID: 9529365 Free PMC article.

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