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Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes.
Abstract
Since 1966, when it first appeared, and through nine editions, McKusick's catalogue has been the definitive reference work on human genetic traits and disorders. Now in two volumes, the tenth edition contains a total of 5,710 entries, 869 more than the ninth, and presents information obtained through March 1, 1992. New in this edition are a guide to the use of OMIM and the genetic code in two alternative easy-to-use formats.
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Citations
Cited by
Genetic Dissection of Complex Traits
Lander, E. S., & Schork, N. J. (1994) · Science · doi:10.1126/science.8091226 · Cited by 3,413
Geisterfer-Lowrance, A. A. T., Kass, S., Tanigawa, G., Vosberg, H.-P., McKenna, W., Seidman, C. E., & Seidman, J. G. (1990) · Cell · doi:10.1016/0092-8674(90)90274-i · Cited by 1,380
Legouis, R., Hardelin, J.-P., Levilliers, J., Claverie, J.-M., Compain, S., Wunderle, V., Millasseau, P., Le Paslier, D., Cohen, D., & Caterina, D. (1991) · Cell · doi:10.1016/0092-8674(91)90193-3 · Cited by 678
The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl Syndrome
Green, J. S., Parfrey, P. S., Harnett, J. D., Farid, N. R., Cramer, B. C., Johnson, G., Heath, O., McManamon, P. J., O'Leary, E., & Pryse-Phillips, W. (1989) · New England Journal of Medicine · doi:10.1056/nejm198910123211503 · Cited by 555
Amplification of the Zfy and Zfx Genes for Sex Identification in Humans, Cattle, Sheep and Goats
Aasen, E., & Medrano, J. F. (1990) · Nature Biotechnology · doi:10.1038/nbt1290-1279 · Cited by 323
Metadata
- Venue
- Annals of Internal Medicine
- Publisher
- American College of Physicians
- Published
- 1967-03-01
- Volume
- 66
- Issue
- 3
- Pages
- 628-629
- ISSN
- 0003-4819 (ISSN-L)
- 1539-3704
- OpenAlex
- W1597901734
- Cited by
- 970
- References
- 0
- FWCI
- 8.97
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. https://app.cochat.ai/papers/10.7326/0003-4819-66-3-628_2
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- Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. (1967). Annals of Internal Medicine. https://doi.org/10.7326/0003-4819-66-3-628_2
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
