Publications by authors named "Hutton M Kearney"

26Publications

Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated.

Prenat Diagn 2020 06 20;40(7):831-837. Epub 2020 Apr 20.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1002/pd.5693DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377435PMC
June 2020

Interstitial 4q Deletion Syndrome Including Causing Pseudohypoaldosteronism.

Mol Syndromol 2020 Jan 21;10(6):327-331. Epub 2019 Dec 21.

Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

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http://dx.doi.org/10.1159/000505279DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995944PMC
January 2020

Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemia.

Hum Pathol 2019 07 26;89:109-114. Epub 2018 Sep 26.

Department of Laboratory Medicine and Pathology, Division of Laboratory Genetics and Genomics, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1016/j.humpath.2018.09.010DOI Listing
July 2019

The Utilization of Chromosomal Microarray Technologies for Hematologic Neoplasms: An ACLPS Critical Review.

Am J Clin Pathol 2018 Oct;150(5):375-384

Department of Laboratory Medicine and Pathology, Division of Laboratory Genetics and Genomics, Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1093/ajcp/aqy076DOI Listing
October 2018

SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq).

Cancer Genet 2018 02 2;221:1-18. Epub 2017 Dec 2.

Center for Individualized Medicine-Biomarker Discovery, Mayo Clinic, Rochester MN, USA; Department of Molecular Medicine, Mayo Clinic, Rochester MN, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cancergen.2017.11.009DOI Listing
February 2018

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

Genet Med 2013 Nov 26;15(11):901-9. Epub 2013 Sep 26.

1] ARUP Laboratories, Salt Lake City, Utah, USA [2] Department of Pathology, University of Utah, Salt Lake City, Utah, USA.

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http://www.nature.com/articles/gim2013129
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http://dx.doi.org/10.1038/gim.2013.129DOI Listing
November 2013

Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations.

Clin Lab Med 2011 Dec 20;31(4):595-613, ix. Epub 2011 Oct 20.

Fullerton Genetics Center, Mission Health System, 267 McDowell Street, Asheville, NC 28803, USA.

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http://dx.doi.org/10.1016/j.cll.2011.08.003DOI Listing
December 2011

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

Genet Med 2011 Jul;13(7):680-5

Fullerton Genetics Center, Mission Health System, 267 McDowell St., Asheville, NC 28803, USA.

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http://dx.doi.org/10.1097/GIM.0b013e3182217a3aDOI Listing
July 2011

Clinical experience with array CGH: case presentations from nine months of practice.

Am J Med Genet A 2006 Oct;140(19):2050-6

Department of Pediatrics, Division of Clinical Genetics, Duke University Medical Center, Durham, North Carolina 27516, USA.

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http://doi.wiley.com/10.1002/ajmg.a.31417
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http://dx.doi.org/10.1002/ajmg.a.31417DOI Listing
October 2006