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Results 1 - 1 of 1 for "3p-" syndrome
  1. FLNB gene 
    ... Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women. ... in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies. Hum Mutat. 2017 May;38( ...
    https://medlineplus.gov/genetics/gene/flnb - Genetics