Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth

Ruti Parvari, S. Mumm, A. Galil, E. Manor, Y. Bar-David, R. Carmi

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Fingerprint

Dive into the research topics of 'Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth'. Together they form a unique fingerprint.

Keyphrases

Biochemistry, Genetics and Molecular Biology