Results
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7821.
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7822.
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7823.
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7824.
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7825.
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7826.
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7827.
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A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome. [electronic resource] by
- Kobayashi, H
- Kasahara, M
- Hino, M
- Yoshimura, H
- Takahara, S
- Ikeda, K
- Son, C
- Iwakura, T
- Yoshimoto, A
- Ishihara, T
- Ogawa, Y
Producer: 20070208
In:
Journal of endocrinological investigation vol. 29
Availability: No items available.
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7828.
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7829.
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7830.
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7831.
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7832.
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7833.
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7834.
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7835.
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7836.
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7837.
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7838.
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7839.
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7840.
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