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Autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly

✍ Scribed by D. Kumar; R. K. Levick


Book ID
115089418
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
534 KB
Volume
30
Category
Article
ISSN
0009-9163

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Autosomal recessive Robinow syndrome (RRS) is a severe skeletal dysplasia with short stature, generalized limb shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. The gene encoding receptor orphan receptor tyrosine kinase 2 (ROR2) is located on chromosome 9