Original language | English |
---|---|
Pages (from-to) | 164-165 |
Number of pages | 2 |
Journal | Journal of Pediatrics |
Volume | 131 |
Issue number | 1 I |
DOIs | |
State | Published - 1997 |
Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11 [3] (multiple letters)
E. Hatchwell, M. C. Johnson, M. S. Watson, S. B. Dowton, A. W. Strauss
Research output: Contribution to journal › Letter › peer-review
5
Scopus
citations