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Diagnostic exome sequencing identifies GLI2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies by Sajan, Samin A.; Powis, Zöe; Helbig, Katherine L.; Nagakura, Honey; Immken, Ladonna; Tang, Sha; Alcaraz, Wendy A. is a Medicine article available to read on EtoBox.

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Author
Sajan, Samin A.; Powis, Zöe; Helbig, Katherine L.; Nagakura, Honey; Immken, Ladonna; Tang, Sha; Alcaraz, Wendy A.
Publisher
Wiley (John Wiley & Sons); John Wiley and Sons Ltd; [Oxford]: John Wiley & Sons Inc, 2013-; Wiley; Research Square (ISSN 2050-0904)
Published
2018
Field
Medicine (Health Sciences)

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