QuickView for CDPX1;jsessionid=13347BBCBAAA9FD89017CAC3B71839EE;jsessionid=5539D0B70788276145B248090B656614;jsessionid=0B8BBCA5F2CE346A2984940457D9B877;jsessionid=F7E60FE16A670661AF09D14D51A7A04F;jsessionid=A0EBD9F861039A8D1816C1ADCEF22FF6 (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. Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that include…
4. Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy prese…
5. A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatas…

There were no clinical trials for CDPX1;jsessionid=13347BBCBAAA9FD89017CAC3B71839EE;jsessionid=5539D0B70788276145B248090B656614;jsessionid=0B8BBCA5F2CE346A2984940457D9B877;jsessionid=F7E60FE16A670661AF09D14D51A7A04F;jsessionid=A0EBD9F861039A8D1816C1ADCEF22FF6