DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Scott AF, Mohr DW, Kasch LM , et al.
Identification of an HMGB3 frameshift mutation in a family with an X-linked colobomatous microphthalmia syndrome using whole-genome and X-exome sequencing.

JAMA Ophthalmol 2014;
132 (10) 1215-1220

Scott AF, Mohr DW, Kasch LM , et al.
Identification of an HMGB3 frameshift mutation in a family with an X-linked colobomatous microphthalmia syndrome using whole-genome and X-exome sequencing.

JAMA Ophthalmol 2014;
132 (10) 1215-1220

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