Xenia Parisi

Xenia Parisi

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Xenia Parisi

Xenia Parisi

Publications by authors named "Xenia Parisi"

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Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype.

PLoS Genet 2019 May 24;15(5):e1008143. Epub 2019 May 24.

NIH Undiagnosed Diseases Program, Common Fund, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.

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http://dx.plos.org/10.1371/journal.pgen.1008143
Publisher Site
http://dx.doi.org/10.1371/journal.pgen.1008143DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534290PMC
May 2019

Impedance to blood flow in the umbilical arteries and infant survival in twin-to-twin transfusion syndrome.

Ultrasound Obstet Gynecol 2019 Apr 22. Epub 2019 Apr 22.

Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX.

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http://dx.doi.org/10.1002/uog.20298DOI Listing
April 2019