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- Q57970194 description "article" @default.
- Q57970194 description "im April 1992 veröffentlichter wissenschaftlicher Artikel" @default.
- Q57970194 description "wetenschappelijk artikel" @default.
- Q57970194 description "наукова стаття, опублікована у квітні 1992" @default.
- Q57970194 name "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 name "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 type Item @default.
- Q57970194 label "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 label "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 prefLabel "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 prefLabel "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 P1433 Q57970194-0B7AE4C6-7432-46C5-8124-209FBEDD7C4E @default.
- Q57970194 P1476 Q57970194-52FEB96D-1A49-4EFE-815E-70BDCAB8AAF0 @default.
- Q57970194 P2093 Q57970194-2C745027-5805-4AB9-A985-D28AD2EF049B @default.
- Q57970194 P2093 Q57970194-50A86CC6-AAE5-4AB1-A642-0966AE57BCA3 @default.
- Q57970194 P2093 Q57970194-7D752B7E-7DAB-47D2-8E2C-1B2425139C49 @default.
- Q57970194 P2093 Q57970194-7F12AD39-7C9D-4422-B673-5CB9B84855C8 @default.
- Q57970194 P2093 Q57970194-F3379E79-77DE-4C5B-90E7-D2554EDC8BC2 @default.
- Q57970194 P304 Q57970194-07F2A2A0-4FD9-4B58-B803-3A8E4D7A60F9 @default.
- Q57970194 P31 Q57970194-15E9D2A0-C5C1-46A8-9F30-084C4CEB949E @default.
- Q57970194 P356 Q57970194-76CD8581-CE27-4B8A-BD71-6D814E5CCFF0 @default.
- Q57970194 P433 Q57970194-8DD4A309-69D2-4AED-9FA3-5792F1C0B4FE @default.
- Q57970194 P478 Q57970194-1687D876-FEF6-4748-8328-33F4E74A2621 @default.
- Q57970194 P50 Q57970194-74FA04BA-66E3-488D-AAA4-989B8CA4320C @default.
- Q57970194 P577 Q57970194-D5613FD7-61A5-4748-8E02-A87247B4C28B @default.
- Q57970194 P698 Q57970194-BE568406-226E-4BDA-A261-93443D514062 @default.
- Q57970194 P921 Q57970194-820FC3ED-CC3B-4BE3-9BA0-F2501A551114 @default.
- Q57970194 P356 AJMG.1320430134 @default.
- Q57970194 P698 1605193 @default.
- Q57970194 P1433 Q15755121 @default.
- Q57970194 P1476 "Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development" @default.
- Q57970194 P2093 "F Rousseau" @default.
- Q57970194 P2093 "I Oberlé" @default.
- Q57970194 P2093 "J Boué" @default.
- Q57970194 P2093 "J L Mandel" @default.
- Q57970194 P2093 "V Biancalana" @default.
- Q57970194 P304 "208-216" @default.
- Q57970194 P31 Q13442814 @default.
- Q57970194 P356 "10.1002/AJMG.1320430134" @default.
- Q57970194 P433 "1-2" @default.
- Q57970194 P478 "43" @default.
- Q57970194 P50 Q39066461 @default.
- Q57970194 P577 "1992-04-01T00:00:00Z" @default.
- Q57970194 P698 "1605193" @default.
- Q57970194 P921 Q928498 @default.