Cody JD - Search Results

1

Molecular characterization of 18p deletions: evidence for a breakpoint cluster.

Schaub RL, Reveles XT, Baillargeon J, Leach RJ, Cody JD. Schaub RL, et al. Among authors: cody jd. Genet Med. 2002 Jan-Feb;4(1):15-9. doi: 10.1097/00125817-200201000-00003. Genet Med. 2002. PMID: 11839953 Free article.

2

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

3

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

4

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

5

Growth hormone insufficiency associated with haploinsufficiency at 18q23.

Cody JD, Hale DE, Brkanac Z, Kaye CI, Leach RJ. Cody JD, et al. Am J Med Genet. 1997 Sep 5;71(4):420-5. Am J Med Genet. 1997. PMID: 9286448

6

Genetic linkage of Paget disease of the bone to chromosome 18q.

Cody JD, Singer FR, Roodman GD, Otterund B, Lewis TB, Leppert M, Leach RJ. Cody JD, et al. Am J Hum Genet. 1997 Nov;61(5):1117-22. doi: 10.1086/301601. Am J Hum Genet. 1997. PMID: 9345096 Free PMC article.

7

Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss.

Keppler-Noreuil KM, Carroll AJ, Finley SC, Descartes M, Cody JD, DuPont BR, Gay CT, Leach RJ. Keppler-Noreuil KM, et al. Among authors: cody jd. Am J Med Genet. 1998 Apr 13;76(5):372-8. doi: 10.1002/(sici)1096-8628(19980413)76:5<372::aid-ajmg2>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9556294

8

Identification of cryptic rearrangements in patients with 18q- deletion syndrome.

Brkanac Z, Cody JD, Leach RJ, DuPont BR. Brkanac Z, et al. Among authors: cody jd. Am J Hum Genet. 1998 Jun;62(6):1500-6. doi: 10.1086/301854. Am J Hum Genet. 1998. PMID: 9585582 Free PMC article.

9

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, …

10

Gene expression patterns in cell lines from patients with 18q- syndrome.

Wang Z, Cody JD, Leach RJ, O'Connell P. Wang Z, et al. Among authors: cody jd. Hum Genet. 1999 Jun;104(6):467-75. doi: 10.1007/s004390050989. Hum Genet. 1999. PMID: 10453734

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