Publications by authors named "Scott D McLean"

11Publications

Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency.

Mol Genet Metab 2020 05 10;130(1):49-57. Epub 2020 Feb 10.

NIH Undiagnosed Diseases Program, Common Fund, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA; Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2020.02.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303973PMC
May 2020

Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries.

Birth Defects Res 2019 11 16;111(18):1356-1364. Epub 2019 Jul 16.

Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas.

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http://dx.doi.org/10.1002/bdr2.1549DOI Listing
November 2019

But is the platter really silver?

Authors:
Scott D McLean

Genet Med 2010 Feb;12(2):126

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http://dx.doi.org/10.1097/GIM.0b013e3181cecd48DOI Listing
February 2010

Spectra of particulate backscattering in natural waters.

Opt Express 2009 Aug;17(18):16192-208

Department of Physics, University of Miami, Coral Gables, FL 33124, USA.

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http://dx.doi.org/10.1364/OE.17.016192DOI Listing
August 2009

Haematopoietic stem cells participate in muscle regeneration.

Br J Haematol 2007 Sep 2;138(6):792-801. Epub 2007 Aug 2.

Roger Williams Medical Center, Department of Research, Providence, RI 02908, USA.

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http://dx.doi.org/10.1111/j.1365-2141.2007.06720.xDOI Listing
September 2007