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The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.
Prenat Diagn. 2011 Aug;31(8):778-87. doi: 10.1002/pd.2766. Epub 2011 Jun 21.
Prenat Diagn. 2011.
PMID: 21692086
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: alliman s.
Prenat Diagn. 2008 Sep;28(9):789-95. doi: 10.1002/pd.2053.
Prenat Diagn. 2008.
PMID: 18646242
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Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.
Coppinger J, Alliman S, Lamb AN, Torchia BS, Bejjani BA, Shaffer LG.
Coppinger J, et al. Among authors: alliman s.
Prenat Diagn. 2009 Dec;29(12):1156-66. doi: 10.1002/pd.2371.
Prenat Diagn. 2009.
PMID: 19795450
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Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2.
Alliman S, Coppinger J, Marcadier J, Thiese H, Brock P, Shafer S, Weaver C, Asamoah A, Leppig K, Dyack S, Morash B, Schultz R, Torchia BS, Lamb AN, Bejjani BA.
Alliman S, et al.
Clin Genet. 2010 Aug;78(2):162-8. doi: 10.1111/j.1399-0004.2010.01373.x. Epub 2010 Feb 9.
Clin Genet. 2010.
PMID: 20345475
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Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
Duker AL, Ballif BC, Bawle EV, Person RE, Mahadevan S, Alliman S, Thompson R, Traylor R, Bejjani BA, Shaffer LG, Rosenfeld JA, Lamb AN, Sahoo T.
Duker AL, et al. Among authors: alliman s.
Eur J Hum Genet. 2010 Nov;18(11):1196-201. doi: 10.1038/ejhg.2010.102. Epub 2010 Jun 30.
Eur J Hum Genet. 2010.
PMID: 20588305
Free PMC article.
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A tale of two deletions: a report of two novel 20p13 --> pter deletions.
McGill AK, Pastore MT, Herman GE, Alliman S, Rosenfeld JA, Weaver DD.
McGill AK, et al. Among authors: alliman s.
Am J Med Genet A. 2010 Apr;152A(4):1000-7. doi: 10.1002/ajmg.a.33339.
Am J Med Genet A. 2010.
PMID: 20358616
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A comparative analysis of ethical and professional challenges experienced by Australian and U.S. genetic counselors.
Alliman S, Veach PM, Bartels DM, Lian F, James C, LeRoy BS.
Alliman S, et al.
J Genet Couns. 2009 Aug;18(4):379-94. doi: 10.1007/s10897-009-9229-9. Epub 2009 May 19.
J Genet Couns. 2009.
PMID: 19452265
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Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization.
Filho AB, Souza J, Faucz FR, Sotomaior VS, Dupont B, Bartel F, Rodriguez R, Schwartz CE, Skinner C, Alliman S, Raskin S.
Filho AB, et al. Among authors: alliman s.
Am J Med Genet A. 2011 May;155A(5):1152-6. doi: 10.1002/ajmg.a.33942. Epub 2011 Apr 11.
Am J Med Genet A. 2011.
PMID: 21485001
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