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European Journal of Human Genetics : EJHG
|
February 16, 2012
TBX5 intragenic duplication: a family with an atypical Holt-Oram syndrome phenotype
Chirag Patel, Lee Silcock, Dominic McMullan, et al.
British Journal of Haematology
|
February 26, 2020
A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies
Julia van Campen, Lee Silcock, Shu Yau, et al.
Scientific Reports
|
July 8, 2021
Human sample authentication in biomedical research: comparison of two platforms
Harshitha Shobha Manjunath, Nicola James, Rebecca Mathew, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2012
17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum
Abhijit Dixit, Chirag Patel, Rachel Harrison, et al.
International Journal of Molecular Sciences
|
November 13, 2025
<i>BTN2A1</i> and <i>BTN3A1</i> as Novel Coeliac Disease Risk Loci: An In Silico Analysis
Kim Ngan Luu Hoang, Shelley Evans, Thomas W Willis, et al.
Cancers
|
August 14, 2020
Utility of Circulating Tumor DNA for Detection and Monitoring of Endometrial Cancer Recurrence and Progression
Esther L Moss, Diviya N Gorsia, Anna Collins, et al.
Clinical Kidney Journal
|
September 9, 2020
Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis
Annalisa Terranegra, Teresa Arcidiacono, Lorenza Macrina, et al.
European Urology Oncology
|
April 12, 2022
Highly Sensitive and Specific Detection of Bladder Cancer via Targeted Ultra-deep Sequencing of Urinary DNA
Douglas G Ward, Laura Baxter, Sascha Ott, et al.
Journal of Translational Medicine
|
April 7, 2019
Monoallelic expression in melanoma
Lee Silcock, Hakeem Almabrazi, Younes Mokrab, et al.
Journal of Translational Medicine
|
May 13, 2020
Differential responsiveness to BRAF inhibitors of melanoma cell lines BRAF V600E-mutated
Muna Al Hashmi, Konduru S Sastry, Lee Silcock, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
European Journal of Human Genetics : EJHG
|
February 16, 2012
TBX5 intragenic duplication: a family with an atypical Holt-Oram syndrome phenotype
Chirag Patel, Lee Silcock, Dominic McMullan, et al.
British Journal of Haematology
|
February 26, 2020
A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies
Julia van Campen, Lee Silcock, Shu Yau, et al.
Scientific Reports
|
July 8, 2021
Human sample authentication in biomedical research: comparison of two platforms
Harshitha Shobha Manjunath, Nicola James, Rebecca Mathew, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2012
17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum
Abhijit Dixit, Chirag Patel, Rachel Harrison, et al.
International Journal of Molecular Sciences
|
November 13, 2025
<i>BTN2A1</i> and <i>BTN3A1</i> as Novel Coeliac Disease Risk Loci: An In Silico Analysis
Kim Ngan Luu Hoang, Shelley Evans, Thomas W Willis, et al.
Cancers
|
August 14, 2020
Utility of Circulating Tumor DNA for Detection and Monitoring of Endometrial Cancer Recurrence and Progression
Esther L Moss, Diviya N Gorsia, Anna Collins, et al.
Clinical Kidney Journal
|
September 9, 2020
Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis
Annalisa Terranegra, Teresa Arcidiacono, Lorenza Macrina, et al.
European Urology Oncology
|
April 12, 2022
Highly Sensitive and Specific Detection of Bladder Cancer via Targeted Ultra-deep Sequencing of Urinary DNA
Douglas G Ward, Laura Baxter, Sascha Ott, et al.
Journal of Translational Medicine
|
April 7, 2019
Monoallelic expression in melanoma
Lee Silcock, Hakeem Almabrazi, Younes Mokrab, et al.
Journal of Translational Medicine
|
May 13, 2020
Differential responsiveness to BRAF inhibitors of melanoma cell lines BRAF V600E-mutated
Muna Al Hashmi, Konduru S Sastry, Lee Silcock, et al.
Page
of 2