ReviewAnnals of the New York Academy of Sciences2017
Postaxial limb hypoplasia (PALH): the classification, clinical features, and related developmental biology.
Review in Annals of the New York Academy of Sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 12 citations in OpenAlex.
- Tibial Plateau Fracture in a Patient with Fibular Hemimelia: A Case Report.Journal of orthopaedic case reports · 2026Article
- Ankle and foot deformities and malformations in proximal femoral focal deficiency.Journal of children's orthopaedics · 2025Article
- Characteristics of terminal hemimelia: What is the difference between terminal hemimelia and classic fibular hemimelia?Journal of children's orthopaedics · 2024Article
- A novel enhancer near theeLife · 2018Article
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Authors and funding
6 authors at 2 institutions in 2 countries.
Funding
Abstract
Postaxial limb hypoplasia (PALH) is a group of nonhereditary diseases with congenital lower limb deficiency affecting the fibular ray, including fibular hemimelia, proximal femoral focal deficiency, and tarsal coalition. The etiology and the developmental biology of the anomaly are still not fully understood. Here, we review the previous classification systems, present the clinical features, and discuss the developmental biology of PALH.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.