Sanger WG - 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: sanger wg. Genet Med. 2008 Apr;10(4):262-6. doi: 10.1097/GIM.0b013e31816b64ad. Genet Med. 2008. PMID: 18414209 Free article.

2

Cytogenetic characterization of diffuse large cell lymphoma using multi-color fluorescence in situ hybridization.

Dave BJ, Nelson M, Pickering DL, Chan WC, Greiner TC, Weisenburger DD, Armitage JO, Sanger WG. Dave BJ, et al. Among authors: sanger wg. Cancer Genet Cytogenet. 2002 Jan 15;132(2):125-32. doi: 10.1016/s0165-4608(01)00548-9. Cancer Genet Cytogenet. 2002. PMID: 11850073

3

Cytogenetics and fluorescence in situ hybridization studies of diffuse large B-cell lymphoma in children and young adults.

Dave BJ, Weisenburger DD, Higgins CM, Pickering DL, Hess MM, Chan WC, Sanger WG. Dave BJ, et al. Among authors: sanger wg. Cancer Genet Cytogenet. 2004 Sep;153(2):115-21. doi: 10.1016/j.cancergencyto.2004.01.008. Cancer Genet Cytogenet. 2004. PMID: 15350300

4

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: sanger wg. 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

5

Role of cytogenetics and molecular cytogenetics in the diagnosis of genetic imbalances.

Dave BJ, Sanger WG. Dave BJ, et al. Among authors: sanger wg. Semin Pediatr Neurol. 2007 Mar;14(1):2-6. doi: 10.1016/j.spen.2006.11.003. Semin Pediatr Neurol. 2007. PMID: 17331878 Review.

6

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: sanger wg. 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

7

Lymphoma cytogenetics.

Dave BJ, Nelson M, Sanger WG. Dave BJ, et al. Among authors: sanger wg. Clin Lab Med. 2011 Dec;31(4):725-61, x-xi. doi: 10.1016/j.cll.2011.08.001. Epub 2011 Oct 21. Clin Lab Med. 2011. PMID: 22118746 Review.

8

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: sanger wg. 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

9

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: sanger wg. 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.

10

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: sanger wg. 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.

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