Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneity
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01314.x/fullpdf
Reference25 articles.
1. Congenital bowing of the long bones in two sisters;Stuve;Lancet,1971
2. Presentation of six cases of Stuve-Wiedemann syndrome;Cormier-Daire;Pediatr Radiol,1998
3. Clinical homogeneity of the Stuve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2;Cormier-Daire;Am J Med Genet,1998
4. Stuve-Wiedemann dysplasia in a 3 1/2-year-old boy;Kozlowski;Am J Med Genet,1996
5. Characterization of a long-term survivor with Stuve-Wiedemann syndrome and mosaicism of a supernumerary marker chromosome;Chen;Am J Med Genet,2001
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1. Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review;Orphanet Journal of Rare Diseases;2022-04-23
2. Influences of the IL-6 cytokine family on bone structure and function;Cytokine;2021-10
3. Oral ulceration in Stüve-Wiedemann syndrome: a new presentation;BMJ Case Reports;2021-08
4. Delineation of the clinical and radiological features of Stuve–Wiedemann syndrome childhood survivors, four new cases and review of the literature;American Journal of Medical Genetics Part A;2020-12-11
5. Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome;Journal of Experimental Medicine;2020-01-08
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