Prenatal diagnosis of Bruck syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference10 articles.
1. Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17
2. Osteogenesis imperfecta with joint contractures: Bruck syndrome
3. Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome) ??? evidence for possible autosomal recessive inheritance
4. Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome)
5. Brack Syndrome
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1. Bruck syndrome in pregnancy;BMJ Case Reports;2024-09
2. Congenital Contractures and Fractures: A Variant of Bruck Syndrome Type 2;Cureus;2024-06-09
3. Pierre Robin Syndrome and a Subglottic Mass in a Patient with Bruck Syndrome: An Unusual Presentation of an Extremely Rare Condition;ENT Updates;2024-03-29
4. Injury with a Metal Cutting Wheel Involving Three Anatomical Regions of the Neck;ENT Updates;2024-03-29
5. Bruck syndrome – description of the first Polish infant with FKBP10 gene mutation;Pediatria i Medycyna Rodzinna;2023-06-30
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