Olney AH - Search Results

1

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations.

Pickering DL, Eudy JD, Olney AH, Dave BJ, Golden D, Stevens J, Sanger WG. Pickering DL, et al. Among authors: olney ah. Genet Med. 2008 Apr;10(4):262-6. doi: 10.1097/GIM.0b013e31816b64ad. Genet Med. 2008. PMID: 18414209 Free article.

2

Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: review of distal 7q deletions.

Rush ET, Stevens JM, Sanger WG, Olney AH. Rush ET, et al. Among authors: olney ah. Am J Med Genet A. 2013 Jul;161A(7):1726-32. doi: 10.1002/ajmg.a.35951. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696251 Review.

3

Cryptic duplication and deletion of 9q34.3 --> qter in a family with a t(9;22)(q34.3;p11.2).

Sanger TM, Olney AH, Zaleski D, Pickering D, Nelson M, Sanger WG, Dave BJ. Sanger TM, et al. Among authors: olney ah. Am J Med Genet A. 2005 Sep 15;138(1):51-5. doi: 10.1002/ajmg.a.30922. Am J Med Genet A. 2005. PMID: 16104013

4

Inherited 14q duplication and 21q deletion: a rare adjacent-2 segregation in multiple family members.

Dave BJ, Olney AH, Zaleski DH, Pickering DL, Becker TA, Chipman HE, Sanger WG. Dave BJ, et al. Among authors: olney ah. Am J Med Genet A. 2009 Oct;149A(10):2248-53. doi: 10.1002/ajmg.a.32999. Am J Med Genet A. 2009. PMID: 19760655

5

Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome.

Sanmann JN, Bishay DL, Starr LJ, Bell CA, Pickering DL, Stevens JM, Kahler SG, Olney AH, Schaefer GB, Sanger WG. Sanmann JN, et al. Among authors: olney ah. Am J Med Genet A. 2012 Jun;158A(6):1285-91. doi: 10.1002/ajmg.a.35347. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581587

6

Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.

Starr LJ, Truemper EJ, Pickering DL, Sanger WG, Olney AH. Starr LJ, et al. Among authors: olney ah. Am J Med Genet A. 2014 Aug;164A(8):2020-4. doi: 10.1002/ajmg.a.34020. Epub 2014 Jun 20. Am J Med Genet A. 2014. PMID: 24954807 Review.

7

Partial deletion of 14q and partial duplication of 14q in sibs: testicular mosaicism for t(14q;14q) as a common mechanism.

Masada CT, Olney AH, Fordyce R, Sanger WG. Masada CT, et al. Among authors: olney ah. Am J Med Genet. 1989 Dec;34(4):528-34. doi: 10.1002/ajmg.1320340415. Am J Med Genet. 1989. PMID: 2624263

8

Occurrence of nephroblastomatosis with dup(18)(q11.2-q23) implicates trisomy 18 tumor screening protocol in select patients with 18q duplication.

Starr LJ, Sanmann JN, Olney AH, Wandoloski M, Sanger WG, Coulter DW. Starr LJ, et al. Among authors: olney ah. Am J Med Genet A. 2014 Apr;164A(4):1079-82. doi: 10.1002/ajmg.a.36432. Epub 2014 Mar 4. Am J Med Genet A. 2014. PMID: 24596125

9

18q22.3 --> 18q23 deletion syndrome and cleft palate.

Eudy JD, Pickering DL, Lutz R, Platt K, Dave BJ, Olney AH, Sanger WG. Eudy JD, et al. Among authors: olney ah. Am J Med Genet A. 2010 Apr;152A(4):1046-8. doi: 10.1002/ajmg.a.33336. Am J Med Genet A. 2010. PMID: 20358626 No abstract available.

10

Partial duplication of distal 17q.

Bridge J, Sanger W, Mosher G, Buehler B, Hearty C, Olney A, Fordyce R. Bridge J, et al. Am J Med Genet. 1985 Oct;22(2):229-35. doi: 10.1002/ajmg.1320220203. Am J Med Genet. 1985. PMID: 4050855

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