Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf

Dorsal (A) and palmar (B) view of the hands of the girl in Figure 1. Note clinodactyly, widened fingertips, and prominent joints.

Figure 2. [Digital anomalies and pectus excavatum in individuals with HYAL2 deficiency]. - GeneReviews® - NCBI Bookshelf

The Ptch1DL mouse: A new model to study lambdoid craniosynostosis and basal cell nevus syndrome‐associated skeletal defects - Feng - 2013 - genesis - Wiley Online Library

PDF) Pachyonychia Congenita Type PC-K6a: The first report in the Vietnamese population

Disorders of Keratinization

Metabolic and Nutritional Disorders Relevant in Dermatology

TGFB3 Gene - GeneCards, TGFB3 Protein

Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues - Romano - 2022 - Birth Defects Research - Wiley Online Library

Independent DSG4 frameshift variants in cats with hair shaft dystrophy

Figure, Flexor tendons and sheath] - StatPearls - NCBI Bookshelf

Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia - ScienceDirect

Classification of congenital upper limb anomalies: towards improved communication, diagnosis, and discovery - Kerby C. Oberg, 2019

PDF) Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence)

A report and review of the recurrent c.811C>T variant and mutation spectrum of Kindler syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 years

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