Showing results 1 to 8 of 8
Title | Author(s) | Issue Date | |
---|---|---|---|
20-Oct-2014 | |||
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong Journal:Clinical and Translational Medicine | 2016 | ||
Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature Journal:American Journal of Medical Genetics, Part A | 2013 | ||
2012 | |||
A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling Journal:European Journal of Medical Genetics | 28-Jan-2014 | ||
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 | ||
2017 | |||
2014 |