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A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype. [electronic resource] by
- Balak, Chris
- Belnap, Newell
- Ramsey, Keri
- Joss, Shelagh
- Devriendt, Koen
- Naymik, Marcus
- Jepsen, Wayne
- Siniard, Ashley L
- Szelinger, Szabolcs
- Parker, Mary E
- Richholt, Ryan
- Izatt, Tyler
- LaFleur, Madison
- Terraf, Panieh
- Llaci, Lorida
- De Both, Matt
- Piras, Ignazio S
- Rangasamy, Sampathkumar
- Schrauwen, Isabelle
- Craig, David W
- Huentelman, Matt
- Narayanan, Vinodh
Producer: 20190520
In:
American journal of medical genetics. Part A vol. 176
Availability: No items available.
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