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American Journal of Medical Genetics, Part A 8
Showing records 1 to 8 |
Display all abstracts in American Journal of Medical Genetics, Part A60487 Anirdia-like phenotype caused by 6p25 dosage aberrationsSadagopan KA
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60301 Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Crow YJ; Chase DS
American Journal of Medical Genetics, Part A 2015; 167: 296-312
60487 Anirdia-like phenotype caused by 6p25 dosage aberrationsLiu GT; Capasso JE
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60301 Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Lowenstein Schmidt J; Szynkiewicz M
American Journal of Medical Genetics, Part A 2015; 167: 296-312
60487 Anirdia-like phenotype caused by 6p25 dosage aberrationsWuthisiri W
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60301 Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Forte GM
American Journal of Medical Genetics, Part A 2015; 167: 296-312
60487 Anirdia-like phenotype caused by 6p25 dosage aberrationsKeep RB; Levin AV
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60301 Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Gornall HL; Oojageer A; Anderson B; Pizzino A; Helman G; Abdel-Hamid MS; Abdel-Salam GM; Ackroyd S; Aeby A; Agosta G; Albin C; Allon-Shalev S; Arellano M; Ariaudo G; Aswani V; Babul-Hirji R
American Journal of Medical Genetics, Part A 2015; 167: 296-312