Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf
Por um escritor misterioso
Last updated 12 janeiro 2025
Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)
Facial features of individuals with proximal and distal truncating
Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families - ScienceDirect
Landmark-Guided Conditional GANs for Face Aging
Age-invariant face recognition using gender specific 3D aging modeling
L11. Anomalies of Facial Development Part I Flashcards
L11. Anomalies of Facial Development Part I Flashcards
Pitt-Hopkins Syndrome - GeneReviews® - NCBI Bookshelf
Pitt-Hopkins Syndrome - GeneReviews® - NCBI Bookshelf
L11. Anomalies of Facial Development Part I Flashcards
Clinical and genomic characterization of 8p cytogenomic disorders - ScienceDirect
A new approach for the analysis of facial growth and age estimation: Iris ratio
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
Congenital Generalized Hypomelanosis and Immunodeficiency in a Black Child - Susan - 2007 - Pediatric Dermatology - Wiley Online Library
Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia
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