Xia, Zhilian

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

Szafranski, P., Schaaf, C. P., Person, R. E., Gibson, I. B., Xia, Z., Mahadevan, S., Wiszniewska, J., Bacino, C. A., Lalani, S., Potocki, L., et al. (2010) · Human Mutation

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 134

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay

Wiśniowiecka‐Kowalnik, B., Nesteruk, M., Peters, S. U., Xia, Z., Cooper, M. L., Savage, S., Amato, R. S., Bader, P., Browning, M. F., Haun, C. L., et al. (2010) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 82

HERV‐mediated genomic rearrangement of EYA1 in an individual with branchio‐oto‐renal syndrome

Sanchez‐Valle, A., Wang, X., Potocki, L., Xia, Z., Kang, S. L., Carlin, M. E., Michel, D., Williams, P., Cabrera‐Meza, G., Brundage, E. K., et al. (2010) · American Journal of Medical Genetics Part A

Genomic variations and chromosomal abnormalitiesCongenital Ear and Nasal Anomalies

Cited by 43