Aarskog syndrome: The changing phenotype with age
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. A familial syndrome of short stature associated with facial dysplasia and genital anomalies
2. Aarskog syndrome: Full male and female expression associated with an X-autosome translocation
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1. FGD1-related Aarskog–Scott syndrome: Identification of four novel variations and a literature review of clinical and molecular aspects;European Journal of Pediatrics;2024-02-27
2. Case Report: Aarskog-scott syndrome caused by FGD1 gene variation: A family study;Frontiers in Genetics;2022-08-16
3. FGD1 Variant Associated With Aarskog–Scott Syndrome;Frontiers in Pediatrics;2022-07-14
4. AARSKOG SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30
5. Aarskog-Scott syndrome: clinical and molecular characterisation of a family with the coexistence of a novel FGD1 mutation and 16p13.11-p12.3 microduplication;BMJ Case Reports;2020-06
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