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Growth hormone deficiency associated in the 18q deletion syndrome.
Ghidoni PD, Hale DE, Cody JD, Gay CT, Thompson NM, McClure EB, Danney MM, Leach RJ, Kaye CI. Ghidoni PD, et al. Among authors: cody jd. Am J Med Genet. 1997 Mar 3;69(1):7-12. doi: 10.1002/(sici)1096-8628(19970303)69:1<7::aid-ajmg2>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9066876
Preferential loss of the paternal alleles in the 18q- syndrome.
Cody JD, Pierce JF, Brkanac Z, Plaetke R, Ghidoni PD, Kaye CI, Leach RJ. Cody JD, et al. Am J Med Genet. 1997 Mar 31;69(3):280-6. doi: 10.1002/(sici)1096-8628(19970331)69:3<280::aid-ajmg12>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9096757
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.
Gay CT, Hardies LJ, Rauch RA, Lancaster JL, Plaetke R, DuPont BR, Cody JD, Cornell JE, Herndon RC, Ghidoni PD, Schiff JM, Kaye CI, Leach RJ, Fox PT. Gay CT, et al. Among authors: cody jd. Am J Med Genet. 1997 Jul 25;74(4):422-31. doi: 10.1002/(sici)1096-8628(19970725)74:4<422::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9259379
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.
Cody JD, Ghidoni PD, DuPont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI. Cody JD, et al. Am J Med Genet. 1999 Aug 27;85(5):455-62. doi: 10.1002/(sici)1096-8628(19990827)85:5<455::aid-ajmg5>3.0.co;2-z. Am J Med Genet. 1999. PMID: 10405442
The estimated frequency is approximately 1/40,000 live births [Cody JD, Pierce JF, Brkanac Z, Plaetke R, Ghidoni PD, Kaye CI, Leach RJ. 1997. ...
The estimated frequency is approximately 1/40,000 live births [Cody JD, Pierce JF, Brkanac Z, Plaetke R, Ghidoni PD, Kaye CI, …
106 results