Katrina Haude

Katrina Haude

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Katrina Haude

Katrina Haude

Publications by authors named "Katrina Haude"

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A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia.

HeartRhythm Case Rep 2016 Jan 13;2(1):32-35. Epub 2015 Oct 13.

University of Rochester School of Medicine and Dentistry, Department of Pediatrics, Division of Pediatric Cardiology.

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http://dx.doi.org/10.1016/j.hrcr.2015.08.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412637PMC
January 2016

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Am J Hum Genet 2015 Aug 30;97(2):343-52. Epub 2015 Jul 30.

Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands. Electronic address:

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https://clinicforspecialchildren.org/wp-content/uploads/2015
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http://linkinghub.elsevier.com/retrieve/pii/S000292971500280
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http://dx.doi.org/10.1016/j.ajhg.2015.07.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573244PMC
August 2015

Analyzing the role of receptor internalization in the regulation of melanin-concentrating hormone signaling.

Int J Endocrinol 2013 17;2013:143052. Epub 2013 Nov 17.

Department of Biology, 217 Lennon Hall, The College at Brockport, State University of New York, 350 New Campus Drive, Brockport, NY 14420, USA.

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http://dx.doi.org/10.1155/2013/143052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855962PMC
December 2013