Results
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12521.
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12522.
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12523.
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12524.
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12525.
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12533.
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12534.
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12535.
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12536.
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De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability. [electronic resource] by
- Parker, Michael J
- Fryer, Alan E
- Shears, Deborah J
- Lachlan, Katherine L
- McKee, Shane A
- Magee, Alex C
- Mohammed, Shehla
- Vasudevan, Pradeep C
- Park, Soo-Mi
- Benoit, Valérie
- Lederer, Damien
- Maystadt, Isabelle
- Study, Ddd
- FitzPatrick, David R
Producer: 20160614
In:
American journal of medical genetics. Part A vol. 167A
Availability: No items available.
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12537.
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12538.
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12539.
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12540.
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