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Viewing 6 Result(s)
Products Available
Catalog IDDescriptionCell TypeCell LineDNAPanelGenotypesSexAgeRacePDL
GM21921ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONSFibroblastYesNA21921NoNoMale15 MOMore than one race3.06
GM23747RETT SYNDROME; RTTB-LymphocyteYesNA23747NoNoFemale9 YRMore than one race 
GM23503RETT SYNDROME; RTTB-LymphocyteYesNA23503NoNoFemale4 YRCaucasian 
GM21916RETT SYNDROME; RTTB-LymphocyteYesInquireNoNoFemale   
GM21913RETT SYNDROME; RTTB-LymphocyteYesNA21913NoNoFemale   
GM23748RETT SYNDROME; RTTB-LymphocyteYesNA23748NoNoFemale More than one race 
Viewing 6 Result(s)