{
    "PMID": "10712195",
    "TI": "Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.",
    "JT": "American journal of human genetics",
    "BTI": "",
    "DP": "2000-03",
    "AU": "Glaser R L, Jiang W, Boyadjiev S A, Tran A K, Zachary A A, Van Maldergem L, Johnson D, Walsh S, Oldridge M, Wall S A, Wilkie A O, Jabs E W"
}