A case of neonatal Jeune syndrome expanding the phenotype
Author:
Affiliation:
1. Neonatal Intensive Care Unit Azienda Istituti Ospitalieri di Cremona Via Concordia 1 26100 Cremona Italy
2. Clinical Genetics Azienda Istituti Ospitalieri di Cremona Via Concordia 1 26100 Cremona Italy
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.85
Reference10 articles.
1. Jeune syndrome: description of 13 cases and a proposal for follow-up protocol
2. Necropsy findings in neonatal asphyxiating thoracic dystrophy.
3. Ciliopathies: an expanding disease spectrum
4. DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III
5. Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19
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