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6781.
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant. [electronic resource] by
- Golzio, Christelle
- Willer, Jason
- Talkowski, Michael E
- Oh, Edwin C
- Taniguchi, Yu
- Jacquemont, Sébastien
- Reymond, Alexandre
- Sun, Mei
- Sawa, Akira
- Gusella, James F
- Kamiya, Atsushi
- Beckmann, Jacques S
- Katsanis, Nicholas
Producer: 20120717
In:
Nature vol. 485
Availability: No items available.
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6782.
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6783.
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6784.
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6785.
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6786.
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6787.
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6788.
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6789.
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6790.
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6791.
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6792.
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6793.
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6794.
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6795.
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6796.
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6797.
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6798.
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6799.
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Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma. [electronic resource] by
- Lehmann, O J
- Ebenezer, N D
- Jordan, T
- Fox, M
- Ocaka, L
- Payne, A
- Leroy, B P
- Clark, B J
- Hitchings, R A
- Povey, S
- Khaw, P T
- Bhattacharya, S S
Producer: 20001214
In:
American journal of human genetics vol. 67
Availability: No items available.
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6800.
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