Search research articles
Contact Us
Filters
Showing results (41-50 of 46) with videos related to
Page
of 5
Sort By:
You have reached the last page of results.
This site can display upto 46 results.
Physics and Imaging in Radiation Oncology
|
November 24, 2025
Quantitative evaluation of apparent diffusion coefficient in a large multi-unit institution
Joshua P Yung, Yao Ding, Ken-Pin Hwang, et al.
American Journal of Human Genetics
|
May 11, 1992
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium
L A Farrer, K M Grundfast, J Amos, et al.
Diagnostics (Basel, Switzerland)
|
July 29, 2023
Automatic Ventriculomegaly Detection in Fetal Brain MRI: A Step-by-Step Deep Learning Model for Novel 2D-3D Linear Measurements
Farzan Vahedifard, H Asher Ai, Mark P Supanich, et al.
American Journal of Medical Genetics
|
August 22, 1997
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia
J W Innis, J H Asher, Y Liang, et al.
American Journal of Human Genetics
|
October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes
L A Farrer, K S Arnos, J H Asher, et al.
Human Genetics
|
July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations
A L DeStefano, L A Cupples, K S Arnos, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Physics and Imaging in Radiation Oncology
|
November 24, 2025
Quantitative evaluation of apparent diffusion coefficient in a large multi-unit institution
Joshua P Yung, Yao Ding, Ken-Pin Hwang, et al.
American Journal of Human Genetics
|
May 11, 1992
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium
L A Farrer, K M Grundfast, J Amos, et al.
Diagnostics (Basel, Switzerland)
|
July 29, 2023
Automatic Ventriculomegaly Detection in Fetal Brain MRI: A Step-by-Step Deep Learning Model for Novel 2D-3D Linear Measurements
Farzan Vahedifard, H Asher Ai, Mark P Supanich, et al.
American Journal of Medical Genetics
|
August 22, 1997
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia
J W Innis, J H Asher, Y Liang, et al.
American Journal of Human Genetics
|
October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes
L A Farrer, K S Arnos, J H Asher, et al.
Human Genetics
|
July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations
A L DeStefano, L A Cupples, K S Arnos, et al.
Page
of 5