SHPRINTZEN-GOLDBERG SYNDROME RESULTS FROM MUTATIONS IN FIBRILLIN-I, NOT MONOSOMY 22Q11

Authors
HATCHWELL E
Citation
E. Hatchwell, SHPRINTZEN-GOLDBERG SYNDROME RESULTS FROM MUTATIONS IN FIBRILLIN-I, NOT MONOSOMY 22Q11, The Journal of pediatrics, 131(1), 1997, pp. 164-164
Citations number
2
Categorie Soggetti
Pediatrics
Journal title
The Journal of pediatrics → ACNP
ISSN journal
00223476
Volume
131
Issue
1
Year of publication
1997
Part
1
Pages
164 - 164
Database
ISI
SICI code
0022-3476(1997)131:1<164:SSRFMI>2.0.ZU;2-B