Showing results 21 to 25 of 25
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Title | Author(s) | Issue Date | |
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Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability Journal:Journal of Medical Genetics | Tan, NBPagnamenta, ATFerla, MPGadian, JChung, BHYChan, MCYFung, LFCook, EGuter, SBoschann, FHeinen, ASchallne, JMignot, CKeren, BWhalen, SSarret, CMittag, DDemmer, LStapleton, RSaida, KMatsumoto, NMiyake, NSheffer, RMor-Shaked, HBarnett, CPByrne, ABScott, HSKraus, ACappuccio, GBrunetti-Pierri, NIorio, RDi Dato, FPais, LSYeung, ATan, TYTaylor, JCChristodoulou, JWhite, S | 2021 | |
Socio-economic burden in patients with rare diseases in Hong Kong Proceeding/Conference:Joint Annual Scientific Meeting 2020 of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN) | 2020 | ||
2003 | |||
1998 | |||
Three-cation intermixed InGaAs/InAlAs quantum well structures and their optical gain properties Proceeding/Conference:Proceedings of SPIE | 1998 |