Kathy J Jakielski

Kathy J Jakielski

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Kathy J Jakielski

Kathy J Jakielski

Publications by authors named "Kathy J Jakielski"

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2019 May 2;10(1):2079. Epub 2019 May 2.

CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada.

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http://dx.doi.org/10.1038/s41467-019-10161-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497626PMC
May 2019

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2019 02 15;10(1):883. Epub 2019 Feb 15.

CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.

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http://dx.doi.org/10.1038/s41467-019-08800-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377600PMC
February 2019

Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders.

Clin Linguist Phon 2019 ;33(8):707-736

a Intellectual and Developmental Disabilities Research Center, Waisman Center , University of Wisconsin-Madison , Madison , WI , USA.

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http://dx.doi.org/10.1080/02699206.2019.1595732DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633911PMC
January 2019

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2018 11 5;9(1):4619. Epub 2018 Nov 5.

CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada.

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http://www.nature.com/articles/s41467-018-06014-6
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http://dx.doi.org/10.1038/s41467-018-06014-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218476PMC
November 2018

Motor-based intervention protocols in treatment of childhood apraxia of speech (CAS).

Curr Dev Disord Rep 2014 Sep;1(3):197-206

Department of Neurology, Mayo Clinic, 200 1st St SW, Rochester, MN 55905, .

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http://dx.doi.org/10.1007/s40474-014-0016-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192721PMC
September 2014

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

J Neurodev Disord 2013 Oct 2;5(1):29. Epub 2013 Oct 2.

Waisman Center, University of Wisconsin-Madison, 1500 Highland Avenue, Madison, WI, 53705, USA.

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http://dx.doi.org/10.1186/1866-1955-5-29DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851280PMC
October 2013

Encoding, memory, and transcoding deficits in Childhood Apraxia of Speech.

Clin Linguist Phon 2012 May;26(5):445-82

Waisman Center, University of Wisconsin-Madison, Madison, WI 53705, USA.

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http://dx.doi.org/10.3109/02699206.2012.655841DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580385PMC
May 2012

Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS).

Am J Med Genet A 2008 Sep;146A(17):2227-33

Waisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.

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http://dx.doi.org/10.1002/ajmg.a.32363DOI Listing
September 2008