QuickView for CDPX1;jsessionid=13347BBCBAAA9FD89017CAC3B71839EE;jsessionid=5539D0B70788276145B248090B656614;jsessionid=0B8BBCA5F2CE346A2984940457D9B877;jsessionid=F7E60FE16A670661AF09D14D51A7A04F;jsessionid=D251C598DC4A7A18BD5FAC16F7EDC891 (gene)

1. Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and …
2. Uniparental disomy as a mechanism for X-linked chondrodysplasia punctata.
3. Predicting the pathogenicity of missense variants based on protein instability to support diagnosis …
4. Oscillometry for personalizing continuous distending pressure maneuvers: an observational study in e…
5. Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that include…

There were no clinical trials for CDPX1;jsessionid=13347BBCBAAA9FD89017CAC3B71839EE;jsessionid=5539D0B70788276145B248090B656614;jsessionid=0B8BBCA5F2CE346A2984940457D9B877;jsessionid=F7E60FE16A670661AF09D14D51A7A04F;jsessionid=D251C598DC4A7A18BD5FAC16F7EDC891