Ballif BC - Search Results

1

aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.

Theisen A, Rosenfeld JA, Farrell SA, Harris CJ, Wetzel HH, Torchia BA, Bejjani BA, Ballif BC, Shaffer LG. Theisen A, et al. Among authors: ballif bc. Am J Med Genet A. 2009 May;149A(5):914-8. doi: 10.1002/ajmg.a.32767. Am J Med Genet A. 2009. PMID: 19353629

2

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, Theisen A, Kashork CD, Shaffer LG. Bejjani BA, et al. Among authors: ballif bc. Am J Med Genet A. 2005 Apr 30;134(3):259-67. doi: 10.1002/ajmg.a.30621. Am J Med Genet A. 2005. PMID: 15723295

3

Array-based comparative genomic hybridization in clinical diagnosis.

Bejjani BA, Theisen AP, Ballif BC, Shaffer LG. Bejjani BA, et al. Among authors: ballif bc. Expert Rev Mol Diagn. 2005 May;5(3):421-9. doi: 10.1586/14737159.5.3.421. Expert Rev Mol Diagn. 2005. PMID: 15934818 Review.

4

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.

Ballif BC, Rorem EA, Sundin K, Lincicum M, Gaskin S, Coppinger J, Kashork CD, Shaffer LG, Bejjani BA. Ballif BC, et al. Am J Med Genet A. 2006 Dec 15;140(24):2757-67. doi: 10.1002/ajmg.a.31539. Am J Med Genet A. 2006. PMID: 17103431

5

Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH.

Ballif BC, Hornor SA, Sulpizio SG, Lloyd RM, Minier SL, Rorem EA, Theisen A, Bejjani BA, Shaffer LG. Ballif BC, et al. Genet Med. 2007 Mar;9(3):150-62. doi: 10.1097/gim.0b013e3180312087. Genet Med. 2007. PMID: 17413419 Free article.

6

The clinical utility of enhanced subtelomeric coverage in array CGH.

Ballif BC, Sulpizio SG, Lloyd RM, Minier SL, Theisen A, Bejjani BA, Shaffer LG. Ballif BC, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1850-7. doi: 10.1002/ajmg.a.31842. Am J Med Genet A. 2007. PMID: 17632771

7

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

Ballif BC, Hornor SA, Jenkins E, Madan-Khetarpal S, Surti U, Jackson KE, Asamoah A, Brock PL, Gowans GC, Conway RL, Graham JM Jr, Medne L, Zackai EH, Shaikh TH, Geoghegan J, Selzer RR, Eis PS, Bejjani BA, Shaffer LG. Ballif BC, et al. Nat Genet. 2007 Sep;39(9):1071-3. doi: 10.1038/ng2107. Epub 2007 Aug 19. Nat Genet. 2007. PMID: 17704777

8

The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.

Shaffer LG, Theisen A, Bejjani BA, Ballif BC, Aylsworth AS, Lim C, McDonald M, Ellison JW, Kostiner D, Saitta S, Shaikh T. Shaffer LG, et al. Among authors: ballif bc. Genet Med. 2007 Sep;9(9):607-16. doi: 10.1097/gim.0b013e3181484b49. Genet Med. 2007. PMID: 17873649 Free article. Review.

9

The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.

Shaffer LG, Bejjani BA, Torchia B, Kirkpatrick S, Coppinger J, Ballif BC. Shaffer LG, et al. Among authors: ballif bc. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):335-45. doi: 10.1002/ajmg.c.30152. Am J Med Genet C Semin Med Genet. 2007. PMID: 17910076 Review.

10

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.

Shaffer LG, Coppinger J, Alliman S, Torchia BA, Theisen A, Ballif BC, Bejjani BA. Shaffer LG, et al. Among authors: ballif bc. Prenat Diagn. 2008 Sep;28(9):789-95. doi: 10.1002/pd.2053. Prenat Diagn. 2008. PMID: 18646242

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

91 results

Search Page

Filters