Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Paul Hillman"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100939- (2024)
Externí odkaz:
https://doaj.org/article/085961c83328412bb087805534d282e6
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101175- (2024)
Externí odkaz:
https://doaj.org/article/9df2a47877794f57b4d3db3a6834f2b0
Autor:
Jordan Zeiger, Paul Hillman
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101272- (2024)
Externí odkaz:
https://doaj.org/article/db3eb2f45dac4a05b573e3197c462463
Publikováno v:
e-Journal of Nondestructive Testing, Vol 28, Iss 8 (2023)
Imaging techniques based on ultrasonic Total Focusing Method (TFM1) are more and more applied for industrial applications. Adoption of the technique has been made easier with the publication of the revised ASME V and ISO 23864 and 23865 standards. TF
Externí odkaz:
https://doaj.org/article/14bfcd685c184e9588bdf336aacb5e93
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100213- (2023)
Externí odkaz:
https://doaj.org/article/39011c4b921049dd83098fedde97f9a4
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100221- (2023)
Externí odkaz:
https://doaj.org/article/f51087cbbe7042c5a5d582c3dbd91452
Autor:
Lingying Liu, Paul Hillman
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100260- (2023)
Externí odkaz:
https://doaj.org/article/454273c6c81a4da2a0633990a861e725
Autor:
Lingying Liu, Paul Hillman
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100259- (2023)
Externí odkaz:
https://doaj.org/article/f43edb982fc942c3939b509e3d624552
Autor:
Mariana Lopez Martinolich, Hope Northrup, Pedro Mancias, Paul Hillman, Kavya Rao, Kate Mowrey
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background Nance‐Horan syndrome (NHS) is a rare X‐linked genetic disorder characterized by ophthalmologic and dental anomalies as well as dysmorphic facies. The clinical phenotype in males includes congenital cataracts, vision loss, micr
Externí odkaz:
https://doaj.org/article/b07e123e7afe44eba40fab20502b987b
Autor:
Paul Hillman, Craig Baker, Luke Hebert, Michael Brown, James Hixson, Allison Ashley‐Koch, Alanna C. Morrison, Hope Northrup, Kit Sing Au
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Neural tube defects (NTDs) are the second most common complex birth defect, yet, our understanding of the genetic contribution to their development remains incomplete. Two environmental factors associated with NTDs are Folate and
Externí odkaz:
https://doaj.org/article/0209ff22ada74b249d679797bfbed3e7