Publications by authors named "Amber N Pursley"

19Publications

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

Am J Hum Genet 2019 12 31;105(6):1102-1111. Epub 2019 Oct 31.

Centre for Reproductive Medicine, Shandong University, Jinan 250021, China; The Key laboratory of Reproductive Endocrinology (Shandong University), Ministry of Education, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Jinan 250021, China; Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200135, China; Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai 200135, China; Hong Kong Branches of Chinese National Engineering Research Centers - Center for Assisted Reproductive Technology and Reproductive Genetics, Hong Kong, China. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.10.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904795PMC
December 2019

Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal Karyotype.

Am J Perinatol 2017 03 17;34(4):340-348. Epub 2016 Aug 17.

Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Lenox-Hill Hospital, New York, New York.

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http://dx.doi.org/10.1055/s-0036-1586501DOI Listing
March 2017

Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.

Genet Med 2016 10 25;18(10):1052-5. Epub 2016 Feb 25.

Department of Obstetrics and Gynecology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.

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http://dx.doi.org/10.1038/gim.2015.216DOI Listing
October 2016

Targeted array CGH as a valuable molecular diagnostic approach: experience in the diagnosis of mitochondrial and metabolic disorders.

Mol Genet Metab 2012 Jun 21;106(2):221-30. Epub 2012 Mar 21.

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

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https://linkinghub.elsevier.com/retrieve/pii/S10967192120010
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http://dx.doi.org/10.1016/j.ymgme.2012.03.005DOI Listing
June 2012

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

Prenat Diagn 2012 Apr;32(4):351-61

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

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http://dx.doi.org/10.1002/pd.3861DOI Listing
April 2012

Utilization of targeted array comparative genomic hybridization, MitoMet, in prenatal diagnosis of metabolic disorders.

Mol Genet Metab 2011 Jun 10;103(2):148-52. Epub 2011 Mar 10.

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

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http://dx.doi.org/10.1016/j.ymgme.2011.03.003DOI Listing
June 2011

Molecular characterization of CPS1 deletions by array CGH.

Mol Genet Metab 2011 Jan 19;102(1):103-6. Epub 2010 Sep 19.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, NAB 2015, Houston, TX 77030, USA.

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http://dx.doi.org/10.1016/j.ymgme.2010.08.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869965PMC
January 2011

Challenges in clinical interpretation of microduplications detected by array CGH analysis.

Am J Med Genet A 2010 May;152A(5):1089-100

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

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http://dx.doi.org/10.1002/ajmg.a.33216DOI Listing
May 2010