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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
Patrick R Gonzales, Erica F Andersen, Teneille R Brown, et al.
The Journal of Investigative Dermatology
|
June 2, 2018
Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type
Xiaolong Alan Zhou, Abner Louissaint, Alexander Wenzel, et al.
Blood Cancer Journal
|
June 18, 2025
Guidelines for the testing and reporting of cytogenetic results for risk stratification of multiple myeloma: a report of the Cancer Genomics Consortium Plasma Cell Neoplasm Working Group
Xinyan Lu, Erica F Andersen, Rahul Banerjee, et al.
Human Mutation
|
March 1, 2020
Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
Rami A Ballout, Cheryl Dickerson, Myra J Wick, et al.
Blood Advances
|
February 9, 2021
Genomic landscape of cutaneous follicular lymphomas reveals 2 subgroups with clinically predictive molecular features
Xiaolong Alan Zhou, Jingyi Yang, Kimberly G Ringbloom, et al.
Blood
|
December 3, 2025
Utility of Peripheral Blood Testing for Detection and Surveillance of Clonal Hematopoiesis in Predisposed Individuals (CH-IPI)
Enrico Attardi, Nathan Gray, Sara Lewis, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
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of 3
Search research articles
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 28 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
Patrick R Gonzales, Erica F Andersen, Teneille R Brown, et al.
The Journal of Investigative Dermatology
|
June 2, 2018
Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type
Xiaolong Alan Zhou, Abner Louissaint, Alexander Wenzel, et al.
Blood Cancer Journal
|
June 18, 2025
Guidelines for the testing and reporting of cytogenetic results for risk stratification of multiple myeloma: a report of the Cancer Genomics Consortium Plasma Cell Neoplasm Working Group
Xinyan Lu, Erica F Andersen, Rahul Banerjee, et al.
Human Mutation
|
March 1, 2020
Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
Rami A Ballout, Cheryl Dickerson, Myra J Wick, et al.
Blood Advances
|
February 9, 2021
Genomic landscape of cutaneous follicular lymphomas reveals 2 subgroups with clinically predictive molecular features
Xiaolong Alan Zhou, Jingyi Yang, Kimberly G Ringbloom, et al.
Blood
|
December 3, 2025
Utility of Peripheral Blood Testing for Detection and Surveillance of Clonal Hematopoiesis in Predisposed Individuals (CH-IPI)
Enrico Attardi, Nathan Gray, Sara Lewis, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Page
of 3