Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Taylor Woodfin"'
Autor:
Taylor Woodfin, Christine Stoops, Joseph B. Philips III, Edward Lose, Fady M. Mikhail, Anna Hurst
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background Koolen‐de Vries (KdV) syndrome is caused by a 17q21.31 deletion leading to clinical symptoms of hypotonia and developmental delay and can present with abnormal hair texture. Menkes disease is an X‐linked recessive inherited di
Externí odkaz:
https://doaj.org/article/770e6d960ee74378b678baee8b9a1ca7
Autor:
Christine Stoops, Joseph B. Philips, Taylor Woodfin, Edward J. Lose, Fady M. Mikhail, Anna C.E. Hurst
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Koolen‐de Vries (KdV) syndrome is caused by a 17q21.31 deletion leading to clinical symptoms of hypotonia and developmental delay and can present with abnormal hair texture. Menkes disease is an X‐linked recessive inherited disease cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::848f7e75dc4c32d62021e0dbe2d9ef7e
https://doi.org/10.1002/mgg3.829
https://doi.org/10.1002/mgg3.829
Autor:
Myriam Peralta-Carcelen, Ariel A. Salas, Vivien Phillips, Taylor Woodfin, Namasivayam Ambalavanan, Waldemar A. Carlo
Background: Many extremely preterm infants have low vitamin D concentrations at birth, but early childhood outcomes after vitamin D supplementation have not been reported. Objective: To determine a dose-response relationship between increasing doses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e07309030bd0c7ae4017b2571bb1be44
https://europepmc.org/articles/PMC5860938/
https://europepmc.org/articles/PMC5860938/
