Webb-Dattani Syndrome
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1855-1
Reference5 articles.
1. Al-Sannaa NA, Pepler A, Al-Abdulwahed HY, Al-Majed SI, Abdi RF, Menzel M, Biskup S (2019) Webb–Dattani Syndrome: report of a Saudi Arabian family with a novel homozygous mutation in the ARNT2 Gene. J Pediatr Neurol 17:071–076
2. Aljasser AA (2020) SAT-062 twins with a homozygous variant of ARNT2, this is a Known Saudi Mutation (KSM) of Webb-Dattani Syndrome. J Endocr Soc 4:SAT-062
3. Hu X, Li L, Zhang H, Hu Z, Li L, Sun M, Liu R (2020) Prenatal diagnosis of a de novo tetrasomy 15q24. 3-25.3: case report and literature review. J Clin Lab Anal 34:e23288
4. Webb EA et al (2013) ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies. Brain 136:3096–3105
5. Zwaveling-Soonawala N et al (2018) Clues for polygenic inheritance of pituitary stalk interruption syndrome from exome sequencing in 20 patients. J Clin Endocrinol Metabol 103:415–428
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