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The Treasury of Human Inheritance

·1936·Journal of the American Medical Association

Abstract

A valuable service both to medical men and to those interested in genetics has been performed by the Galton Laboratory of the University of London in compiling the series of publications known collectively as the "Treasury of Human Inheritance." The study on the inheritance of peroneal atrophy brings together a large amount of material and crystallizes knowledge concerning the heredity of this interesting malady. The age of onset was found by Bell to vary widely, each affected family providing a study in itself and tending to have its individual characteristics from the point of view of clinical symptoms, resulting disability, and age of onset. It is interesting to note that individuals of the same sibship tend to be affected at about the same period, often in the same year, of life. Attention is called to the fact that in some cases the first symptoms may be noted in the hands

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Metadata

Venue
Journal of the American Medical Association
Published
1936-07-04
Volume
107
Issue
1
Pages
68
ISSN
0002-9955 (ISSN-L)
OpenAlex
W4205659337
Cited by
161
References
0
FWCI
1.83
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The Treasury of Human Inheritance. https://app.cochat.ai/papers/10.1001/jama.1936.02770270070031
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The Treasury of Human Inheritance. (1936). Journal of the American Medical Association. https://doi.org/10.1001/jama.1936.02770270070031

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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.