Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf
Por um escritor misterioso
Last updated 21 março 2025
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK114458/bin/fhs-Image002.jpg)
Dorsal (A) and palmar (B) view of the hands of the girl in Figure 1. Note clinodactyly, widened fingertips, and prominent joints.
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://journals.physiology.org/cms/10.1152/physrev.00047.2021/asset/images/medium/physrev.00047.2021_f011.gif)
Human temperature regulation under heat stress in health, disease, and injury
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41586-022-05682-1/MediaObjects/41586_2022_5682_Fig3_HTML.png)
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK65895/bin/CDR0000624959.jpg)
Genetics of Skin Cancer (PDQ®) - PDQ Cancer Information Summaries - NCBI Bookshelf
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://onlinelibrary.wiley.com/cms/asset/b9c1710c-0651-4dac-a41e-f5a6562a057d/dvg22416-fig-0004-m.jpg)
The Ptch1DL mouse: A new model to study lambdoid craniosynostosis and basal cell nevus syndrome‐associated skeletal defects - Feng - 2013 - genesis - Wiley Online Library
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://ars.els-cdn.com/content/image/1-s2.0-S0002929713001687-gr3.jpg)
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia - ScienceDirect
CRbook, PDF, Dementia
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://onlinelibrary.wiley.com/cms/asset/5620fe83-ea63-4135-a751-6ba93eb90548/ana26459-gra-0006-m.png)
51st Annual Meeting of the Child Neurology Society - 2022 - Annals of Neurology - Wiley Online Library
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/lw685/springer-static/image/chp%3A10.1007%2F978-3-030-84168-3_2/MediaObjects/19287_6_En_2_Fig23a_HTML.jpg)
The Perinatal Autopsy
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://ars.els-cdn.com/content/image/1-s2.0-S0002929713001687-gr2.jpg)
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia - ScienceDirect
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41586-022-05682-1/MediaObjects/41586_2022_5682_Fig1_HTML.png)
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://onlinelibrary.wiley.com/cms/asset/454f2103-1fd3-46b9-bbb1-fbdc1bd2c243/bdr22113-fig-0001-m.jpg)
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
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://pub.mdpi-res.com/ijms/ijms-24-13962/article_deploy/html/images/ijms-24-13962-g007.png?1694577913)
IJMS, Free Full-Text
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://www.researchgate.net/publication/376508423/figure/fig2/AS:11431281212281399@1702590152273/Simplified-model-for-Hh-signalling-pathway-a-In-absence-of-the-Hh-ligands-PTCH1_Q320.jpg)
PDF) A novel pathogenic splice-site variant in the PTCH1 gene c.3549+1G>T, associated with Gorlin syndrome: a case report
![Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41586-022-05682-1/MediaObjects/41586_2022_5682_Fig4_HTML.png)
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases
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