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Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate loci. [electronic resource] by
- Casley, W L
- Allon, M
- Cousin, H K
- Ting, S S
- Crackower, M A
- Hashimoto, L
- Cornélis, F
- Beckmann, J S
- Hudson, A J
- Ebers, G C
Producer: 19921201
In:
Genomics vol. 14
Availability: No items available.
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14.
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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. [electronic resource] by
- Crackower, M A
- Scherer, S W
- Rommens, J M
- Hui, C C
- Poorkaj, P
- Soder, S
- Cobben, J M
- Hudgins, L
- Evans, J P
- Tsui, L C
Producer: 19970604
In:
Human molecular genetics vol. 5
Availability: No items available.
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15.
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Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development. [electronic resource] by
- Mo, R
- Freer, A M
- Zinyk, D L
- Crackower, M A
- Michaud, J
- Heng, H H
- Chik, K W
- Shi, X M
- Tsui, L C
- Cheng, S H
- Joyner, A L
- Hui, C
Producer: 19970224
In:
Development (Cambridge, England) vol. 124
Availability: No items available.
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16.
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The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. [electronic resource] by
- Kobayashi, K
- Sinasac, D S
- Iijima, M
- Boright, A P
- Begum, L
- Lee, J R
- Yasuda, T
- Ikeda, S
- Hirano, R
- Terazono, H
- Crackower, M A
- Kondo, I
- Tsui, L C
- Scherer, S W
- Saheki, T
Producer: 19990629
In:
Nature genetics vol. 22
Availability: No items available.
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