|
Brunetti-Pierri, Nicola; Lachman, Ralph; Lee, Kwanghyuk et al. (2010) Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region. Am J Med Genet A 152A:1825-31
|
|
Kondkar, A A; Bray, M S; Leal, S M et al. (2010) VAMP8/endobrevin is overexpressed in hyperreactive human platelets: suggested role for platelet microRNA. J Thromb Haemost 8:369-78
|
|
Eichler, Evan E; Flint, Jonathan; Gibson, Greg et al. (2010) Missing heritability and strategies for finding the underlying causes of complex disease. Nat Rev Genet 11:446-50
|
|
Chishti, Muhammad S; Bhatti, Attya; Tamim, Sana et al. (2008) Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. J Hum Genet 53:101-5
|
|
Oosterhuis, Bronson E; LaForge, K Steven; Proudnikov, Dmitri et al. (2008) Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women. Am J Med Genet B Neuropsychiatr Genet 147B:793-8
|
