Results
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1121.
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1123.
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1125.
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1126.
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1127.
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1128.
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1129.
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1130.
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1131.
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1134.
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1135.
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1136.
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1137.
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Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndrome. [electronic resource] by
- Steel, Dora
- Salpietro, Vincenzo
- Phadke, Rahul
- Pitt, Matthew
- Gentile, Giulia
- Massoud, Ahmed
- Batten, Leigh
- Bashamboo, Anu
- Mcelreavey, Ken
- Saggar, Anand
- Kinali, Maria
Producer: 20161103
In:
Journal of genetics vol. 94
Availability: No items available.
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1138.
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1139.
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1140.
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