Results
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6861.
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6862.
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Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly. [electronic resource] by
- Bear, Kelly A
- Solomon, Benjamin D
- Antonini, Sonir
- Arnhold, Ivo J P
- França, Marcela M
- Gerkes, Erica H
- Grange, Dorothy K
- Hadley, Donald W
- Jääskeläinen, Jarmo
- Paulo, Sabrina S
- Rump, Patrick
- Stratakis, Constantine A
- Thompson, Elizabeth M
- Willis, Mary
- Winder, Thomas L
- Jorge, Alexander A L
- Roessler, Erich
- Muenke, Maximilian
Producer: 20150121
In:
Journal of medical genetics vol. 51
Availability: No items available.
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6863.
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6864.
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6865.
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6866.
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6867.
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6868.
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6869.
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6870.
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6871.
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6872.
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6873.
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6874.
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6875.
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6876.
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6877.
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6878.
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6879.
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6880.
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