Cardiovascular abnormalities associated with the Stuve-Wiedemann syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference7 articles.
1. Neonatal Schwartz-Jampel syndrome: a common autosomal recessive syndrome in the United Arab Emirates.
2. Characterization of a long-term survivor with St�ve-Wiedemann syndrome and mosaicism of a supernumerary marker chromosome
3. Clinical homogeneity of the St�ve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2
4. Stüve-Wiedemann dysplasia in a 3 1/2-year-old boy
5. CONGENITAL BOWING OF THE LONG BONES IN TWO SISTERS
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1. Mutations in LIFR rewire the JAK/STAT signaling pathway: A study unveiling mechanistic details of Stüve-Wiedemann syndrome;Computers in Biology and Medicine;2024-09
2. Case Report: Stüve–Wiedemann syndrome—a rare cause of persistent pulmonary hypertension of the newborn;Frontiers in Pediatrics;2024-01-04
3. Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review;Orphanet Journal of Rare Diseases;2022-04-23
4. Stüve-Wiedemann syndrome with a novel mutation in a Saudi infant;International Journal of Pediatrics and Adolescent Medicine;2021-10
5. Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies;Human Molecular Genetics;2020-03-16
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