Publications by authors named "Blake C Ballif"

80Publications

Canine factor VII deficiency: lessons learned in applying methods-based laboratory proficiency testing.

J Vet Diagn Invest 2019 Mar 19;31(2):276-279. Epub 2019 Jan 19.

Genetic Veterinary Sciences Inc., Paw Print Genetics, Spokane, WA.

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http://dx.doi.org/10.1177/1040638718825281DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838828PMC
March 2019

Standards and guidelines for canine clinical genetic testing laboratories.

Hum Genet 2019 May 13;138(5):493-499. Epub 2018 Nov 13.

Paw Print Genetics, Genetic Veterinary Sciences, Inc., 220 E Rowan, Suite 220, Spokane, WA, 99207, USA.

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http://link.springer.com/10.1007/s00439-018-1954-4
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http://dx.doi.org/10.1007/s00439-018-1954-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536461PMC
May 2019

An International Genetic Survey of Breed-Specific Diseases in Working Dogs from the United States, Israel, and Poland.

Cytogenet Genome Res 2017 9;153(4):198-204. Epub 2018 Feb 9.

Paw Print Genetics, Genetic Veterinary Sciences, Inc., Spokane, WA, USA.

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http://dx.doi.org/10.1159/000486774DOI Listing
April 2018

Large inverted duplications in the human genome form via a fold-back mechanism.

PLoS Genet 2014 Jan 30;10(1):e1004139. Epub 2014 Jan 30.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1004139DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907307PMC
January 2014

The use of cytogenetic microarrays in myelodysplastic syndrome characterization.

Methods Mol Biol 2013 ;973:69-85

Signature Genomic Laboratories, PerkinElmer Inc., Spokane, WA, USA.

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http://link.springer.com/content/pdf/10.1007/978-1-62703-281
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http://dx.doi.org/10.1007/978-1-62703-281-0_5DOI Listing
July 2013

Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis.

Genet Med 2012 Nov 5;14(11):914-21. Epub 2012 Jul 5.

1] Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington, USA.

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http://dx.doi.org/10.1038/gim.2012.77DOI Listing
November 2012

The use of new technologies in the detection of balanced translocations in hematologic disorders.

Curr Opin Genet Dev 2012 Jun 13;22(3):264-71. Epub 2012 Feb 13.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, WA, USA.

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http://dx.doi.org/10.1016/j.gde.2012.01.005DOI Listing
June 2012

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Hum Mol Genet 2011 Oct 4;20(19):3769-78. Epub 2011 Jul 4.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1093/hmg/ddr293DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168286PMC
October 2011

The use of microarray technology for cytogenetics.

Methods Mol Biol 2010 ;632:125-39

Signature Genomic Laboratories, Spokane, WA, USA.

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http://dx.doi.org/10.1007/978-1-60761-663-4_8DOI Listing
June 2010

In the middle of it all: a centered approach to chromosome analysis.

Expert Opin Med Diagn 2008 Feb;2(2):221-9

Signature Genomic Laboratories, 120 N Pine St, Spokane, WA 99202, USA +1 509 474 6840 ; +1 509 474 6839 ;

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http://dx.doi.org/10.1517/17530059.2.2.221DOI Listing
February 2008

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

Am J Med Genet C Semin Med Genet 2007 Nov;145C(4):335-45

Signature Genomic Laboratories, LLC, 120 N Pine Street, Ste 242C, Spokane, WA 99202, USA.

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http://dx.doi.org/10.1002/ajmg.c.30152DOI Listing
November 2007

The clinical utility of enhanced subtelomeric coverage in array CGH.

Am J Med Genet A 2007 Aug;143A(16):1850-7

Signature Genomic Laboratories, LLC, Spokane, Washington 99202, USA.

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http://dx.doi.org/10.1002/ajmg.a.31842DOI Listing
August 2007

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

Am J Med Genet A 2006 Dec;140(24):2757-67

Signature Genomic Laboratories, LLC, Spokane, Washington, USA.

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http://dx.doi.org/10.1002/ajmg.a.31539DOI Listing
December 2006

Comparative genomic hybridization by microarray for the detection of cytogenetic imbalance.

Methods Mol Med 2006 ;128:23-31

Health Research and Education Center, Washington State University, Spokane, WA, USA.

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http://dx.doi.org/10.1007/978-1-59745-159-8_3DOI Listing
December 2006

Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.

Eur J Hum Genet 2006 Dec 30;14(12):1255-62. Epub 2006 Aug 30.

Health Research and Education Center, Washington State University Spokane, Spokane, WA 99210, USA.

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http://www.sld.cu/galerias/pdf/sitios/genetica/translocacion
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http://www.nature.com/doifinder/10.1038/sj.ejhg.5201710
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http://dx.doi.org/10.1038/sj.ejhg.5201710DOI Listing
December 2006

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.

Hum Genet 2006 Nov 18;120(4):519-26. Epub 2006 Jul 18.

Health Research and Education Center, Washington State University Spokane, Spokane, WA, 99210-1495, USA.

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http://dx.doi.org/10.1007/s00439-006-0222-1DOI Listing
November 2006

Array-based comparative genomic hybridization in clinical diagnosis.

Expert Rev Mol Diagn 2005 May;5(3):421-9

Signature Genomic Laboratories, 44 West 6th Avenue, Suite 202, Spokane, WA 99204, USA.

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http://dx.doi.org/10.1586/14737159.5.3.421DOI Listing
May 2005

Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions.

Chromosome Res 2004 ;12(2):133-41

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

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http://dx.doi.org/10.1023/b:chro.0000013165.88969.10DOI Listing
September 2004

Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.

Hum Mol Genet 2003 Sep 15;12(17):2153-65. Epub 2003 Jul 15.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

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http://dx.doi.org/10.1093/hmg/ddg231DOI Listing
September 2003