Browse by Author Huizenga, J
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| Title | Author(s) | Year | View Count |  | Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy | Minassian, BA; Lee Jeffrey, R; Herbrick, JA; Huizenga, J; Soder, S; Mungall, AJ; Dunham, I; Gardner, R; Fong, CYG; Carpenter, S; Jardim, L; Satishchandra, P; Andermann, E; Carter Snead III, O; LopesCendes, I; Tsui, LC; DelgadoEscueta, AV; Rouleau, GA; Scherer, SW | 1998 | 648 |
| Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients | Osborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC | 1996 | 296 |
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