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GeneReviews, an international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families. Each chapter in GeneReviews is written by one or more experts on the specific condition or disease and goes through a rigorous editing and peer review process before being published online.
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Hex Code
Color name
RGB
HSL
CMYK
#20558A
Blumine
32, 85, 138
210, 62, 33
77, 38, 0, 46
#F9F9F9
Alabaster
249, 249, 249
0, 0, 98
0, 0, 0, 2
#000000
Black
0, 0, 0
0, 0, 0
0, 0, 0, 100
NCBI's GeneReviews is a renowned brand that provides an international point-of-care resource for clinicians. It offers a comprehensive range of clinically relevant and medically actionable information on inherited conditions. This valuable resource is presented in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.
Each chapter in GeneReviews is meticulously written by experts specializing in specific conditions or diseases. Before being published online, these chapters undergo a rigorous editing and peer review process. With over 870 chapters currently available, GeneReviews attracts more than five million users annually.
The content on GeneReviews is divided into two main formats: chapters focusing on individual genes or phenotypes (~95%) and overviews summarizing common genetic conditions such as deafness and hearing loss, and Alzheimer's disease (~5%). To ensure up-to-date and accurate information, each chapter is periodically updated every four to five years by the authors, with additional revisions made as necessary. GeneReviews remains a trusted resource for clinicians, providing invaluable guidance for the management of inherited conditions and promoting the well-being of patients and their families
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Health
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