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Cancer Genetics
|
May 13, 2019
FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancer
Jaime L Lopes, Sophia Chaudhry, Guilherme S Lopes, et al.
Prenatal Diagnosis
|
April 11, 2020
Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated
Jaime L Lopes, Guilherme S Lopes, Elizabeth A L Enninga, et al.
Gastrointestinal Disorders (Basel, Switzerland)
|
November 7, 2024
The Innate Immune System Surveillance Biomarker p87 in African Americans and Caucasians with Small High-Grade Dysplastic Adenoma [SHiGDA] and Right-Sided <i>JAK3</i> Colon Mutations May Explain the Presence of Multiple Cancers Revealing an Important Minority of Patients with <i>JAK3</i> Mutations and Colorectal Neoplasia
Martin Tobi, Xiaoqing Zhao, Rebecca Rodriquez, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2023
Uniparental disomy of multiple chromosomes in two cases with a complex phenotype
Katarzyna Polonis, Jaime L Lopes, Huong Cabral, et al.
The Pharmacogenomics Journal
|
February 1, 2022
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota
Guilherme S Lopes, Jaime L Lopes, Suzette J Bielinski, et al.
Cancer Genetics
|
April 10, 2020
Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis
Jaime L Lopes, Matthew Webley, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD
|
January 18, 2022
Targeted Genotyping in Clinical Pharmacogenomics: What Is Missing?
Jaime L Lopes, Kimberley Harris, Mary Beth Karow, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Cancer Genetics
|
May 13, 2019
FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancer
Jaime L Lopes, Sophia Chaudhry, Guilherme S Lopes, et al.
Prenatal Diagnosis
|
April 11, 2020
Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated
Jaime L Lopes, Guilherme S Lopes, Elizabeth A L Enninga, et al.
Gastrointestinal Disorders (Basel, Switzerland)
|
November 7, 2024
The Innate Immune System Surveillance Biomarker p87 in African Americans and Caucasians with Small High-Grade Dysplastic Adenoma [SHiGDA] and Right-Sided <i>JAK3</i> Colon Mutations May Explain the Presence of Multiple Cancers Revealing an Important Minority of Patients with <i>JAK3</i> Mutations and Colorectal Neoplasia
Martin Tobi, Xiaoqing Zhao, Rebecca Rodriquez, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2023
Uniparental disomy of multiple chromosomes in two cases with a complex phenotype
Katarzyna Polonis, Jaime L Lopes, Huong Cabral, et al.
The Pharmacogenomics Journal
|
February 1, 2022
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota
Guilherme S Lopes, Jaime L Lopes, Suzette J Bielinski, et al.
Cancer Genetics
|
April 10, 2020
Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis
Jaime L Lopes, Matthew Webley, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD
|
January 18, 2022
Targeted Genotyping in Clinical Pharmacogenomics: What Is Missing?
Jaime L Lopes, Kimberley Harris, Mary Beth Karow, et al.
Page
of 1