The DOI matches its Crossref record.
The Treasury of Human Inheritance
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
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia
Geoffroy, G., Barbeau, A., Breton, G., Lemieux, B., Aube, M., Leger, C., & Bouchard, J. P. (1976) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100025464 · Cited by 379
Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1
Gao, B., Guo, J., She, C., Shu, A., Yang, M., Tan, Z., Yang, X., Guo, S., Feng, G., & He, L. (2001) · Nature Genetics · doi:10.1038/ng577 · Cited by 271
Temtamy, S. A., & Aglan, M. S. (2008) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-3-15 · Cited by 158
Metadata
- Venue
- Journal of the American Medical Association
- Publisher
- American Medical Association (AMA)
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: The Treasury of Human Inheritance. https://app.cochat.ai/papers/10.1001/jama.1936.02770270070031
- The paper
- The Treasury of Human Inheritance. (1936). Journal of the American Medical Association. https://doi.org/10.1001/jama.1936.02770270070031
Data sources
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.