Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders

Mendelian Inheritance in Man (MIM) is a comprehensive, authoritative, and timely genetic knowledgebase that serves clinical medicine and biomedical research.

With over 2,000 new entries and a total of more than 9,000 entries, MIM provides the most up-to-date information on genetic disorders and neoplasms, including mapping information on more than 4,000 genes of known function.

This book is a must-have for clinical geneticists, researchers, and anyone involved in the field of human genetics.

Its comprehensive coverage and timeliness make it an essential resource for understanding the complex relationships between genetics and disease.