Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf
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Last updated 13 abril 2025
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK114458/bin/fhs-Image001.jpg)
Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)
Facial features of individuals with proximal and distal truncating
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fejhg.2014.156/MediaObjects/41431_2015_Article_BFejhg2014156_Fig4_HTML.jpg)
Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://ars.els-cdn.com/content/image/1-s2.0-S1098360021051765-gr2.jpg)
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families - ScienceDirect
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/lw685/springer-static/image/chp%3A10.1007%2F978-3-031-06427-2_23/MediaObjects/532577_1_En_23_Fig3_HTML.png)
Landmark-Guided Conditional GANs for Face Aging
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11042-019-7694-1/MediaObjects/11042_2019_7694_Fig5_HTML.png)
Age-invariant face recognition using gender specific 3D aging modeling
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://o.quizlet.com/AfD8DAGhYEv63U-3bIGM2g.png)
L11. Anomalies of Facial Development Part I Flashcards
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://o.quizlet.com/QCwKw0yLD8QybvOP7wplyQ.png)
L11. Anomalies of Facial Development Part I Flashcards
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK100240/bin/pitt-hopkins-Image001.gif)
Pitt-Hopkins Syndrome - GeneReviews® - NCBI Bookshelf
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK100240/bin/pitt-hopkins-Image005.gif)
Pitt-Hopkins Syndrome - GeneReviews® - NCBI Bookshelf
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://quizlet.com/cdn-cgi/image/f=auto,fit=cover,h=200,onerror=redirect,w=240/https://o.quizlet.com/yoCu6W7Ptz7A.G5bMxaacQ.png)
L11. Anomalies of Facial Development Part I Flashcards
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://ars.els-cdn.com/content/image/1-s2.0-S1098360021054496-gr3.jpg)
Clinical and genomic characterization of 8p cytogenomic disorders - ScienceDirect
A new approach for the analysis of facial growth and age estimation: Iris ratio
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://onlinelibrary.wiley.com/cms/asset/4feab385-690a-4dc8-b6c8-9f37313bb629/ajmg.a.v176.12.cover.jpg?trick=1702008814868)
The oculoauriculofrontonasal syndrome: Further clinical characterization and additional evidence suggesting a nontraditional mode of inheritance - Lehalle - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://onlinelibrary.wiley.com/cms/asset/29e28466-268d-4830-b1f2-4fea684e676c/j.1525-1470.2007.00371.x.fp.png)
Congenital Generalized Hypomelanosis and Immunodeficiency in a Black Child - Susan - 2007 - Pediatric Dermatology - Wiley Online Library
![Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41431-022-01088-9/MediaObjects/41431_2022_1088_Fig1_HTML.png)
Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia
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