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Showing 1-1 of 1 result for "200-735-9" within Papers
Sevjidmaa Baasanjav et al.
BMC medical genetics, 11, 110-110 (2010-07-14)
Osteopoikilosis is a rare autosomal dominant genetic disorder, characterised by the occurrence of the hyperostotic spots preferentially localized in the epiphyses and metaphyses of the long bones, and in the carpal and tarsal bones 1. Heterozygous LEMD3 gene mutations were
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