Education:
MD, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China 1998
Board Certification(s):
American Board of Medical Genetics and Genomics (ABMGG)
- Clinical Molecular Genetics and Genomics
- Clinical Cytogenetics and Genomics
Clinical/Research Interests:
Clinical Genetic Testing
Molecular Basis of Mendelian Disorders
Cancer Genetics
Select Publications:
Pang, H. (2020). Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1. Frontires in Genetics. PMID: 32655619. DOI: 10.3389/fgene.2020.00577
Wang, X., Pang, H., Shah, B. A., Gu, H., Zhang, L., Wang, H. (2020). A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation. (vol. 8, pp. 88). Frontiers in pediatrics. PMID: 32211354. DOI: 10.3389/fped.2020.00088
Gao, M., Pang, H., Kim, Y. M., Lu, X., Wang, X., Lee, J., Wang, M., Meng, F., Li, S. (2019). An extra chromosome 9 derived from either a normal chromosome 9 or a derivative chromosome 9 in a patient with acute myeloid leukemia positive for t(9;11)(p21.3;q23.3): A case report. Oncology letters, 18(6), 6725-6731. PMID: 31807181. DOI: 10.3892/ol.2019.11035