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7 in total

1. Spondylocostal dysostosis.

Authors: I D Young; J R Moore
Journal: J Med Genet Date: 1984-02 Impact factor: 6.318

2. A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Authors: P D Turnpenny; M P Bulman; T M Frayling; T K Abu-Nasra; C Garrett; A T Hattersley; S Ellard
Journal: Am J Hum Genet Date: 1999-07 Impact factor: 11.025

3. Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.

Authors: P D Turnpenny; N Whittock; J Duncan; S Dunwoodie; K Kusumi; S Ellard
Journal: J Med Genet Date: 2003-05 Impact factor: 6.318

4. Spondylocostal dysostosis and urinary tract anomaly: definition and review of an entity.

Authors: E A Devos; J G Leroy; J J Braeckman; L J Vanden Bulcke; L O Langer
Journal: Eur J Pediatr Date: 1978-05-22 Impact factor: 3.183

5. Hereditary costovertebral dysplasia with malignant cerebral tumour.

Authors: T J David; A Glass
Journal: J Med Genet Date: 1983-12 Impact factor: 6.318

6. Congenital spinal deformity in a three generation family.

Authors: I K Temple; T G Thomas; M Baraitser
Journal: J Med Genet Date: 1988-12 Impact factor: 6.318

7. Evidence for variable gene expression in a large inbred kindred with autosomal recessive spondylocostal dysostosis.

Authors: P D Turnpenny; R J Thwaites; F N Boulos
Journal: J Med Genet Date: 1991-01 Impact factor: 6.318

7 in total