Search research articles
Contact Us
Filters
Showing results (71-80 of 97) with videos related to
Page
of 10
Sort By:
Clinical Epigenetics
|
March 17, 2022
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Thomas Eggermann, Elzem Yapici, Jet Bliek, et al.
Deutsches Arzteblatt International
|
March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare Diseases
Miriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
Hemasphere
|
October 19, 2022
Impaired Overall Survival in Young Patients With Acute Myeloid Leukemia and Variants in Genes Predisposing for Myeloid Malignancies
Martin Kirschner, Benjamin Rolles, Martina Crysandt, et al.
Epigenomics
|
June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances
Susanne Bens, Julia Kolarova, Jasmin Beygo, et al.
Blood Cancer Journal
|
January 6, 2026
Frequent and clinically relevant germline DNA repair gene variants in young and familial myeloproliferative neoplasms
Robert Meyer, Maria Jimena Rodriguez, Madeline Caduc, et al.
Leukemia
|
May 12, 2018
Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita
Martin Kirschner, Angela Maurer, Marcin W Wlodarski, et al.
European Journal of Human Genetics : EJHG
|
May 12, 2016
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome
Katja Eggermann, Jet Bliek, Frédéric Brioude, et al.
Hemasphere
|
April 25, 2023
Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria
Mareike Tometten, Martin Kirschner, Robert Meyer, et al.
Brain : a Journal of Neurology
|
August 12, 2020
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles
Carola Hedberg-Oldfors, Robert Meyer, Kay Nolte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 10, 2026
Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4
Philip Harrer, Volker Kittke, Alice Saparov, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 97) with videos related to
Sort By:
Page
of 10
Clinical Epigenetics
|
March 17, 2022
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Thomas Eggermann, Elzem Yapici, Jet Bliek, et al.
Deutsches Arzteblatt International
|
March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare Diseases
Miriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
Hemasphere
|
October 19, 2022
Impaired Overall Survival in Young Patients With Acute Myeloid Leukemia and Variants in Genes Predisposing for Myeloid Malignancies
Martin Kirschner, Benjamin Rolles, Martina Crysandt, et al.
Epigenomics
|
June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances
Susanne Bens, Julia Kolarova, Jasmin Beygo, et al.
Blood Cancer Journal
|
January 6, 2026
Frequent and clinically relevant germline DNA repair gene variants in young and familial myeloproliferative neoplasms
Robert Meyer, Maria Jimena Rodriguez, Madeline Caduc, et al.
Leukemia
|
May 12, 2018
Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita
Martin Kirschner, Angela Maurer, Marcin W Wlodarski, et al.
European Journal of Human Genetics : EJHG
|
May 12, 2016
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome
Katja Eggermann, Jet Bliek, Frédéric Brioude, et al.
Hemasphere
|
April 25, 2023
Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria
Mareike Tometten, Martin Kirschner, Robert Meyer, et al.
Brain : a Journal of Neurology
|
August 12, 2020
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles
Carola Hedberg-Oldfors, Robert Meyer, Kay Nolte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 10, 2026
Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4
Philip Harrer, Volker Kittke, Alice Saparov, et al.
Page
of 10