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References in periodicals archive ?
Santaolalla-Caballero et al., "Heterozygous NPR2 mutations cause disproportionate short stature, similar to Leri-Weill dyschondrosteosis," The Journal of Clinical Endocrinology & Metabolism, vol.
Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome.
LMD is caused by homozygous mutations in the SHOX/SHOXY (short stature homoebox) gene, of which bi-allelic mutations or gross deletions cause Leri-Weill dyschondrosteosis (LWD).