Ehlers-Danlos syndrome: a new oculo-scoliotic type with associated polyneuropathy?
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02916.x/fullpdf
Reference14 articles.
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3. Molecular basis of clinical heterogeneity in Ehlers-Danlos syndrome;Byers;Am. NY. Acad. Sci.,1985
4. Phenotypic Ehlers-Danlos, type VI with normal lysyl hydroxylase activity and macrocephaly;Cadle;Am. J. Hum. Genet.,1985
5. Inherited human collagen lysyl hydroxylase deficiency: ascorbic acid response;Elsas;J. Pediatr.,1978
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