Results
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701.
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702.
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703.
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De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. [electronic resource] by
- Okur, Volkan
- Cho, Megan T
- Henderson, Lindsay
- Retterer, Kyle
- Schneider, Michael
- Sattler, Shannon
- Niyazov, Dmitriy
- Azage, Meron
- Smith, Sharon
- Picker, Jonathan
- Lincoln, Sharyn
- Tarnopolsky, Mark
- Brady, Lauren
- Bjornsson, Hans T
- Applegate, Carolyn
- Dameron, Amy
- Willaert, Rebecca
- Baskin, Berivan
- Juusola, Jane
- Chung, Wendy K
Producer: 20170621
In:
Human genetics vol. 135
Availability: No items available.
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704.
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705.
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706.
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707.
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708.
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709.
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710.
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711.
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712.
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713.
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714.
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715.
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716.
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717.
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718.
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719.
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720.
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