Search research articles
Contact Us
Filters
Showing results (421-430 of 585) with videos related to
Page
of 59
Sort By:
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
November 2, 2005
Prospective, randomized, multicenter, double-blind placebo-controlled trial comparing adjuvant interferon alfa and isotretinoin with interferon alfa alone in stage IIA and IIB melanoma: European Cooperative Adjuvant Melanoma Treatment Study Group
Erika Richtig, H Peter Soyer, Martin Posch, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2018
Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability
Aida M Bertoli-Avella, Jose M Garcia-Aznar, Oliver Brandau, et al.
Neurology. Clinical Practice
|
February 13, 2018
Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update
Marc C Patterson, Peter Clayton, Paul Gissen, et al.
Breast Cancer Research and Treatment
|
May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centers
Christopher Schroeder, Ulrike Faust, Marc Sturm, et al.
Nature
|
October 14, 2011
A draft genome of Yersinia pestis from victims of the Black Death
Kirsten I Bos, Verena J Schuenemann, G Brian Golding, et al.
Brain : a Journal of Neurology
|
April 12, 2026
DRD1-driven infantile dystonia: towards a mechanism-informed framework for GPCR receptoropathies
Gülsüm Kayhan, Ryosuke Tany, Reza Maroofian, et al.
Orphanet Journal of Rare Diseases
|
March 19, 2013
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum
Matthis Synofzik, Anne S Soehn, Janina Gburek-Augustat, et al.
Annals of Neurology
|
July 12, 2002
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype
Ingrid Bauer, Martin Gencik, Franco Laccone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian population
Asha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Brain : a Journal of Neurology
|
May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrum
Inès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Page
of 59
Search research articles
Search
Showing results (421-430 of 585) with videos related to
Sort By:
Page
of 59
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
November 2, 2005
Prospective, randomized, multicenter, double-blind placebo-controlled trial comparing adjuvant interferon alfa and isotretinoin with interferon alfa alone in stage IIA and IIB melanoma: European Cooperative Adjuvant Melanoma Treatment Study Group
Erika Richtig, H Peter Soyer, Martin Posch, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2018
Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability
Aida M Bertoli-Avella, Jose M Garcia-Aznar, Oliver Brandau, et al.
Neurology. Clinical Practice
|
February 13, 2018
Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update
Marc C Patterson, Peter Clayton, Paul Gissen, et al.
Breast Cancer Research and Treatment
|
May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centers
Christopher Schroeder, Ulrike Faust, Marc Sturm, et al.
Nature
|
October 14, 2011
A draft genome of Yersinia pestis from victims of the Black Death
Kirsten I Bos, Verena J Schuenemann, G Brian Golding, et al.
Brain : a Journal of Neurology
|
April 12, 2026
DRD1-driven infantile dystonia: towards a mechanism-informed framework for GPCR receptoropathies
Gülsüm Kayhan, Ryosuke Tany, Reza Maroofian, et al.
Orphanet Journal of Rare Diseases
|
March 19, 2013
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum
Matthis Synofzik, Anne S Soehn, Janina Gburek-Augustat, et al.
Annals of Neurology
|
July 12, 2002
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype
Ingrid Bauer, Martin Gencik, Franco Laccone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian population
Asha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Brain : a Journal of Neurology
|
May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrum
Inès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Page
of 59