Zobrazeno 1 - 4
of 4
pro vyhledávání: '"S. Malia Fullerton"'
Autor:
Bryan A. Comstock, David L. Veenstra, Peter Tarczy-Hornoch, S. Malia Fullerton, Robin L. Bennett, Deborah A. Nickerson, Carlos J. Gallego, Wylie Burke, Caroline S. Bennette, Martha Horike-Pyne, Patrick J. Heagerty, Susan Brown Trinidad, Laura M. Amendola, Dean A. Regier, Michael O. Dorschner, Gail P. Jarvik, Fuki M. Hisama, Donald L. Patrick, William M. Grady
Publikováno v:
Contemporary clinical trials. 39(1)
Whole exome and whole genome sequencing are applications of next generation sequencing transforming clinical care, but there is little evidence whether these tests improve patient outcomes or if they are cost effective compared to current standard of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7429a8ea5aa132303c7ba11830485f39
https://pubmed.ncbi.nlm.nih.gov/24997220
https://pubmed.ncbi.nlm.nih.gov/24997220
Autor:
Kenneth M. Weiss, S Malia Fullerton
Publikováno v:
The Quarterly Review of Biology. 77:244-244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef06b00122e66516c910e166c37ada05
https://doi.org/10.1086/344034
https://doi.org/10.1086/344034
Autor:
Vaibhav Patel, Marc S. Williams, Gail P. Jarvik, Iftikhar J. Kullo, David Carrell, Zi Ye, Angelika Erwin, Marylyn D. Ritchie, S. Malia Fullerton, Elisha M. Friesema, Catherine A. McCarty, Agnes S. Sundaresan, Helena Kuivaniemi, Gabriella Papa, Kimberly Derr, Kris Hansen, Murray H. Brilliant, Sharon Aufox, Carlos J. Gallego, Joseph Bochenek, Amber A. Burt, Paul K. Crane, Sarah C. Stallings, Arno G. Motulsky, Jennifer A. Pacheco, Erwin P. Bottinger, Eric B. Larson, Gerard Tromp, Mariza de Andrade, Terrie Kitchner, David R. Crosslin, Dan M. Roden, Christopher G. Shaw, Brittany Knick Ragon, Maureen E. Smith, Joshua C. Denny, Omri Gottesman, Glenn S. Gerhard
Publikováno v:
The American Journal of Human Genetics. (4):512-520
Hereditary hemochromatosis (HH) is a common autosomal-recessive disorder associated with pathogenic HFE variants, most commonly those resulting in p.Cys282Tyr and p.His63Asp. Recommendations on returning incidental findings of HFE variants in individ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55fe1bb89d0f04e314d4d61da22a3761
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