shox 46 - shox gene mutation : 2024-11-01 shox 46The short-stature homeobox gene (SHOX), also known as short-stature-homeobox-containing gene, is a gene located on both the X and Y chromosomes, which is .
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shox 46The designation SHOX was derived from 'Short stature HOmeoboX-containing gene.'. The 2 mRNAs identified by Rao et al. (1997) contained 1,870 (SHOXa) and 1,349 (SHOXb) .shox gene mutationSHOX is a gene (short stature homeobox-containing gene), which plays an important role in bone growth and development. SHOX deficiency as a result of SHOX gene .
shox 46Feb 4, 2011 — SHOX – the short stature homeobox-containing gene – was discovered by deletion mapping of the short arm of chromosome X by Rao et al. and independently by .The short-stature homeobox gene (SHOX), also known as short-stature-homeobox-containing gene, is a gene located on both the X and Y chromosomes, which is .Nov 8, 2006 — MLPA analysis demonstrated the heterozygous deletion of SHOX in seven patients (46.6%), disclosing the presence of two different proximal breakpoints.
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shox 46