Tanya N Eble

Tanya N Eble

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Tanya N Eble

Tanya N Eble

Publications by authors named "Tanya N Eble"

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14Publications

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Genetic Testing Experiences Among Parents of Children with Autism Spectrum Disorder in the United States.

J Autism Dev Disord 2019 Dec;49(12):4821-4833

Department of Health and Kinesiology, Texas A&M University, College Station, TX, USA.

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http://dx.doi.org/10.1007/s10803-019-04200-zDOI Listing
December 2019

Needs assessment in genetic testing education: A survey of parents of children with autism spectrum disorder in the united states.

Autism Res 2019 Aug 4;12(8):1162-1170. Epub 2019 Jun 4.

Department of Health and Kinesiology, Texas A&M University, College Station, Texas.

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http://dx.doi.org/10.1002/aur.2152DOI Listing
August 2019

A case report of hamartomatous polyposis in an individual with Neurofibromatosis type 1.

Clin Case Rep 2019 Jan 11;7(1):202-205. Epub 2018 Dec 11.

Baylor College of Medicine Houston Texas.

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http://dx.doi.org/10.1002/ccr3.1908DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333055PMC
January 2019

Quality improvement of clinic flow for complex genetic conditions: Using Ehlers-Danlos syndrome as a model.

Mol Genet Genomic Med 2018 11 26;6(6):993-1000. Epub 2018 Sep 26.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.

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http://dx.doi.org/10.1002/mgg3.472DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305640PMC
November 2018

Adult presentation of X-linked Conradi-Hünermann-Happle syndrome.

Am J Med Genet A 2015 Jun 2;167(6):1309-14. Epub 2015 Apr 2.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.

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http://dx.doi.org/10.1002/ajmg.a.36899DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449285PMC
June 2015

Variable levels of tissue mosaicism can confound the interpretation of chromosomal microarray results from peripheral blood.

Eur J Med Genet 2014 May-Jun;57(6):264-6. Epub 2014 Mar 15.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Medicine, Baylor College of Medicine, Houston, TX, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.03.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859793PMC
February 2015

A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14.

Am J Med Genet A 2013 Apr 26;161A(4):841-4. Epub 2013 Feb 26.

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

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http://doi.wiley.com/10.1002/ajmg.a.35751
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http://dx.doi.org/10.1002/ajmg.a.35751DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868782PMC
April 2013

The practice of adult genetics: a 7-year experience from a single center.

Am J Med Genet A 2013 Jan 13;161A(1):89-93. Epub 2012 Dec 13.

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

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http://doi.wiley.com/10.1002/ajmg.a.35684
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http://dx.doi.org/10.1002/ajmg.a.35684DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859647PMC
January 2013

Ophthalmologic findings in Aicardi syndrome.

J AAPOS 2012 Jun;16(3):238-41

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

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http://dx.doi.org/10.1016/j.jaapos.2012.01.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650611PMC
June 2012

A genome-wide screen for copy number alterations in Aicardi syndrome.

Am J Med Genet A 2009 Oct;149A(10):2113-21

Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.32976DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640635PMC
October 2009

Non-random X chromosome inactivation in Aicardi syndrome.

Hum Genet 2009 Mar 1;125(2):211-6. Epub 2009 Jan 1.

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

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http://dx.doi.org/10.1007/s00439-008-0615-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660246PMC
March 2009

Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia.

Nat Genet 2007 Jul 3;39(7):836-8. Epub 2007 Jun 3.

Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1038/ng2057DOI Listing
July 2007

Facial and physical features of Aicardi syndrome: infants to teenagers.

Am J Med Genet A 2005 Oct;138A(3):254-8

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

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http://dx.doi.org/10.1002/ajmg.a.30963DOI Listing
October 2005