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Paper Details

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.
Hum Mutat
105
2018
Author NameAffiliation
Kristy LeeUniversity of North Carolina at Chapel Hill
F??tima CarneiroIstituto de Investigacao e Inovacao em Saude & Ipatimup, Institute of Molecular Pathology and Immunology of the University of Porto
F??tima CarneiroIstituto de Investigacao e Inovacao em Saude & Ipatimup, Institute of Molecular Pathology and Immunology of the University of Porto
David G HuntsmanUniversity of British Columbia
David G HuntsmanUniversity of British Columbia
Pardeep KaurahUniversity of British Columbia
Pardeep KaurahUniversity of British Columbia
Chimene KesserwanSt. Jude Children's Research Hospital
Carla OliveiraIstituto de Investigacao e Inovacao em Saude & Ipatimup, Institute of Molecular Pathology and Immunology of the University of Porto
Amanda B SpurdleQIMR Berghofer Medical Research Institute
Amanda B SpurdleQIMR Berghofer Medical Research Institute
Liying ZhangMemorial Sloan Kettering Cancer Center
Sharon E PlonBaylor College of Medicine
Kasmintan A SchraderUniversity of British Columbia
Kasmintan A SchraderUniversity of British Columbia
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink