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26041.
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26042.
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26043.
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26044.
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26056.
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26057.
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26058.
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PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis. [electronic resource] by
- Macchia, P E
- Lapi, P
- Krude, H
- Pirro, M T
- Missero, C
- Chiovato, L
- Souabni, A
- Baserga, M
- Tassi, V
- Pinchera, A
- Fenzi, G
- Grüters, A
- Busslinger, M
- Di Lauro, R
Producer: 19980529
In:
Nature genetics vol. 19
Availability: No items available.
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26059.
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Mutations in the integrin alpha7 gene cause congenital myopathy. [electronic resource] by
- Hayashi, Y K
- Chou, F L
- Engvall, E
- Ogawa, M
- Matsuda, C
- Hirabayashi, S
- Yokochi, K
- Ziober, B L
- Kramer, R H
- Kaufman, S J
- Ozawa, E
- Goto, Y
- Nonaka, I
- Tsukahara, T
- Wang, J Z
- Hoffman, E P
- Arahata, K
Producer: 19980529
In:
Nature genetics vol. 19
Availability: No items available.
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26060.
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Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood. [electronic resource] by
- Dunger, D B
- Ong, K K
- Huxtable, S J
- Sherriff, A
- Woods, K A
- Ahmed, M L
- Golding, J
- Pembrey, M E
- Ring, S
- Bennett, S T
- Todd, J A
Producer: 19980529
In:
Nature genetics vol. 19
Availability: No items available.
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