| Title | Author(s) | Year | View Count |
 | Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24 | Crackower, MA; Sinasac, DS; Lee, JR; Herbrick, JA; Tsui, LC; Scherer, SW | 1999 | 124 |
 | Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human | Crackower, MA; Snasac, DS; Xia, J; Motoyama, J; Prochazka, M; Rommens, JM; Sbherer, SW; Tsui, LC | 1999 | 222 |
| The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein | Kobayashi, K; Sinasac, DS; Iijima, M; Boright, AP; Begum, L; Lee, JR; Yasuda, T; Ikeda, S; Hirano, R; Terazono, H; Crackower, MA; Kondo, I; Tsui, LC; Scherer, SW; Saheki, T | 1999 | 290 |
| Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue | Sinasac, DS; Crackower, MA; Lee, JR; Kobayashi, K; Saheki, T; Scherer, SW; Tsui, LC | 1999 | 298 |
| Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13 | Crackower, MA; Heng, HHQ; Tsui, LC | 1998 | 110 |
| Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse | Crackower, MA; Motoyama, J; Tsui, LC | 1998 | 280 |
| Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis | Motoyama, J; Heng, H; Crackower, MA; Takabatake, T; Takeshima, K; Tsui, LC; Hui, CC | 1998 | 237 |
| Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6 | Crackower, MA; Heng, HHQ; Shi, X; Scherer, SW; Tsui, LC | 1997 | 96 |
| Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14 | Crackower, MA; Scherer, SW; Heng, HHQ; Tsui, LC | 1997 | 114 |
| Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development | Mo, R; Freer, AM; Zinyk, DL; Crackower, MA; Michaud, J; Heng, HHQ; Chik, KW; Shi, XM; Tsui, LC; Cheng, SH; Joyner, AL; Hui, CC | 1997 | 163 |
| Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development | Crackower, MA; Scherer, SW; Rommens, JM; Hui, CC; Poorkaj, P; Soder, S; Cobben, JM; Hudgins, L; Evans, JP; Tsui, LC | 1996 | 631 |
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