De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome - Concepedia

Concepedia

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De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

DOI Full Paper Access

162

Citations

19

References

2013

Year

Matthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski, Brett H. Graham, Wei Chen, Karen W. Gripp, Kim Jenny, Thomas F. Wienker,

Genome Medicine

References

	Year	Citations

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