The DOI matches its Crossref record.
THE PIERRE ROBIN SYNDROME
Abstract
The whole object of the medical and nursing care of infants with the Pierre Robin syndrome is to keep them alive and thriving in their perilous passage through the early months of life until the failure of mandibular development in utero is subsequently rectified by nature. From my limited experience of this condition I suggest that surgery has little to offer in the treatment of the Pierre Robin syndrome. Cap suspension, tube feeding, and skilled nursing are more important than any surgical procedures.
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
Congenital anomalies in the newborninfant, including minor variations
Marden, P. M., Smith, D. W., & McDonald, M. J. (1964) · The Journal of Pediatrics · doi:10.1016/s0022-3476(64)80188-8 · Cited by 422
Control of genioglossus muscle inspiratory activity
Brouillette, R. T., & Thach, B. T. (1980) · Journal of Applied Physiology · doi:10.1152/jappl.1980.49.5.801 · Cited by 228
Airway Management in Babies With Micrognathia: The Case Against Early Distraction
Chigurupati, R., & Myall, R. (2005) · Journal of Oral and Maxillofacial Surgery · doi:10.1016/j.joms.2005.04.011 · Cited by 20
Metadata
- Authors
- Dennison, W. M.
- Venue
- Pediatrics
- Publisher
- American Academy of Pediatrics (AAP)
- Published
- 1965-09-01
- Volume
- 36
- Issue
- 3
- Pages
- 336-341
- ISSN
- 0031-4005 (ISSN-L)
- 1098-4275
- OpenAlex
- W4206828531
- Cited by
- 432
- References
- 0
- FWCI
- 2.14
- 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 PIERRE ROBIN SYNDROME. https://app.cochat.ai/papers/10.1542/peds.36.3.336
- The paper
- Dennison, W. M. (1965). THE PIERRE ROBIN SYNDROME. Pediatrics. https://doi.org/10.1542/peds.36.3.336
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.