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Human Mutation
|
May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizures
Julian Schubert, Roberta Paravidino, Felicitas Becker, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 24, 2026
Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancer
Natalie Herold, Christoph Engel, Dorothee Speiser, et al.
JCI Insight
|
October 5, 2023
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, et al.
NPJ Precision Oncology
|
October 20, 2023
Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients
Michael Menzel, Stephan Ossowski, Sebastian Kral, et al.
Molecular Psychiatry
|
May 6, 2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.
Neuro-Oncology Advances
|
March 14, 2023
Clinical outcome of biomarker-guided therapies in adult patients with tumors of the nervous system
Mirjam Renovanz, Sylvia C Kurz, Johannes Rieger, et al.
American Journal of Medical Genetics. Part A
|
February 8, 2017
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Tim Ripperger, Stefan S Bielack, Arndt Borkhardt, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 18, 2024
Benchmarking whole exome sequencing in the German network for personalized medicine
Michael Menzel, Mihaela Martis-Thiele, Hannah Goldschmid, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 78) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 78 results.
Human Mutation
|
May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizures
Julian Schubert, Roberta Paravidino, Felicitas Becker, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 24, 2026
Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancer
Natalie Herold, Christoph Engel, Dorothee Speiser, et al.
JCI Insight
|
October 5, 2023
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, et al.
NPJ Precision Oncology
|
October 20, 2023
Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients
Michael Menzel, Stephan Ossowski, Sebastian Kral, et al.
Molecular Psychiatry
|
May 6, 2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.
Neuro-Oncology Advances
|
March 14, 2023
Clinical outcome of biomarker-guided therapies in adult patients with tumors of the nervous system
Mirjam Renovanz, Sylvia C Kurz, Johannes Rieger, et al.
American Journal of Medical Genetics. Part A
|
February 8, 2017
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Tim Ripperger, Stefan S Bielack, Arndt Borkhardt, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 18, 2024
Benchmarking whole exome sequencing in the German network for personalized medicine
Michael Menzel, Mihaela Martis-Thiele, Hannah Goldschmid, et al.
Page
of 8