Hing, Anne V.

Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations

Seto, M. L., Hing, A. V., Chang, J., Hu, M., Kapp‐Simon, K. A., Patel, P. K., Burton, B. K., Kane, A. A., Smyth, M. D., Hopper, R., et al. (2007) · American Journal of Medical Genetics Part A

Craniofacial Disorders and Treatmentsdental development and anomalies

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New scaphocephaly severity indices of sagittal craniosynostosis: A comparative study with cranial index quantifications

Ruiz-Correa, S., Sze, R. W., Starr, J. R., Lin, H.-T. J., Speltz, M. L., Cunningham, M. L., & Hing, A. V. (2006) · The Cleft Palate-Craniofacial Journal

Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment

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Copy number variation analysis in single‐suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis

Mefford, H. C., Shafer, N., Antonacci, F., Tsai, J. M., Park, S. S., Hing, A. V., Rieder, M. J., Smyth, M. D., Speltz, M. L., Eichler, E. E., et al. (2010) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsGenomic variations and chromosomal abnormalities

Cited by 78

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Kobren, S. N., Baldridge, D., Velinder, M., Krier, J. B., LeBlanc, K., Esteves, C., Pusey, B. N., Züchner, S., Blue, E., Lee, H., et al. (2021) · Genetics in Medicine

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

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