Showing results 1 to 7 of 7
| Title | Author(s) | Issue Date | |
|---|---|---|---|
| 2007 | |||
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 | ||
| 2008 | |||
Prenatal diagnosis of a cavernous angioma associated with intracranial hemorrhage: Report of one case and review of the literature [3] Journal:Ultrasound in Obstetrics and Gynecology | 2004 | ||
Successful outcome after serial amnioreductions in triplet fetofetal transfusion syndrome Journal:Obstetrics and Gynecology | 2003 | ||
Mak, CMLaw, ECLee, HHSiu, WKChow, KMAu Yeung, SKNgan, HYSTse, NKKwong, NSChan, GCLee, KWChan, WPWong, SFTang, MHKan, ASHui, APSo, PLShek, CCLee, RSWong, KYYau, EKPoon, KHSiu, SPoon, GWKwok, AMNg, JWYim, VCMa, GGChu, CHTong, TYChong, YKChen, SPChing, CKChan, AOTam, SLau, RLNg, WFLee, KCChan, AYLam, CW | 2018 | ||
Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax Journal:Prenatal Diagnosis | 1999 |