Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Brent Hafen"'
Autor:
Samantha Greenberg, Saundra S. Buys, Sandra L. Edwards, Whitney Espinel, Alison Fraser, Amanda Gammon, Brent Hafen, Kimberly A. Herget, Wendy Kohlmann, Camille Roundy, Carol Sweeney
Publikováno v:
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Abstract Background Personal cancer diagnosis and family cancer history factor into which individuals should undergo genetic testing for hereditary breast and ovarian cancer (HBOC) syndrome. Family history is often determined in the research setting
Externí odkaz:
https://doaj.org/article/3f74e0ad364245f5a1cd9bb163cbe299
Autor:
Nephi A. Walton, Brent Hafen, Sara Graceffo, Nykole Sutherland, Melanie Emmerson, Rachel Palmquist, Christine M. Formea, Maricel Purcell, Bret Heale, Matthew A. Brown, Christopher J. Danford, Sumathi I. Rachamadugu, Thomas N. Person, Katherine A. Shortt, G. Bryce Christensen, Jared M. Evans, Sharanya Raghunath, Christopher P. Johnson, Stacey Knight, Viet T. Le, Jeffrey L. Anderson, Margaret Van Meter, Teresa Reading, Derrick S. Haslem, Ivy C. Hansen, Betsey Batcher, Tyler Barker, Travis J. Sheffield, Bhaskara Yandava, David P. Taylor, Pallavi Ranade-Kharkar, Christopher C. Giauque, Kenneth R. Eyring, Jesse W. Breinholt, Mickey R. Miller, Payton R. Carter, Jason L. Gillman, Andrew W. Gunn, Kirk U. Knowlton, Joshua L. Bonkowsky, Kari Stefansson, Lincoln D. Nadauld, Howard L. McLeod
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 11, p 1867 (2022)
The clinical use of genomic analysis has expanded rapidly resulting in an increased availability and utility of genomic information in clinical care. We have developed an infrastructure utilizing informatics tools and clinical processes to facilitate
Externí odkaz:
https://doaj.org/article/8b0660b1dc4e4da79aa63cdd53ff0344
Autor:
Saundra S. Buys, Brent Hafen, Samantha Greenberg, Alison Fraser, Sandra L. Edwards, Kimberly Herget, Wendy Kohlmann, Whitney Espinel, Amanda Gammon, Carol Sweeney, Camille Roundy
Publikováno v:
Cancer Medicine
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Background Personal cancer diagnosis and family cancer history factor into which individuals should undergo genetic testing for hereditary breast and ovarian cancer (HBOC) syndrome. Family history is often determined in the research setting through k
Publikováno v:
Journal of Genetic Counseling. 18:395-400
In order to evaluate the utility of genetic counseling at the time of first trimester screening in patients with no previously identified genetic concerns, we reviewed family history data for 700 women seen for genetic counseling in Utah during 2005-
Publikováno v:
Prenatal Diagnosis. 33:242-244
Objective First-trimester aneuploidy screening has high detection rates and low false-positive rates. Their use as well as the implementation of non-invasive prenatal testing may affect specialty training in prenatal diagnosis procedures. Study desig
Autor:
David A. Wada, Anne Kennedy, Janice L. B. Byrne, Juliana G. Szakacs, John M. Opitz, L. Brent Hafen
Publikováno v:
Fetal and Pediatric Pathology. 23:159-170
In 1990 Marles and Chudley reported on an infant with absent ulnae and concomitant radial hypoplasia, oligodactyly, hydropsfetalis, and apparent endocardial fibroelastosis (EFE) and, on the basis of phenotype and parental consanguinity, postulated au
Publikováno v:
Prenatal diagnosis. 33(3)
First-trimester aneuploidy screening has high detection rates and low false-positive rates. Their use as well as the implementation of non-invasive prenatal testing may affect specialty training in prenatal diagnosis procedures.Descriptive study of f
Autor:
Nancy C. Rose, L. Brent Hafen
Publikováno v:
Fetal diagnosis and therapy. 28(1)
Publikováno v:
American Journal of Obstetrics and Gynecology. 204:S287
Autor:
Wada, David A., Szakacs, Juliana, Kennedy, Anne M., Brent Hafen, L., Opitz, John M., Byrne, Janice L.
Publikováno v:
Fetal & Pediatric Pathology; Mar-Jun2004, Vol. 23 Issue 2/3, p159-170, 12p