Chromosomal-Abnormalities.md

@@ -14,9 +14,10 @@
 <td>Klinefelter Syndrome (47,XXY)</td>
 <td> <span dir="">GRCh38 (chrX:p)add</span></td>
 <td> 
--  Identifier: CAAB267958021
--  Look up via identifier: https://reg.clinicalgenome.org/allele/CAAB267958021
--  Look up via descriptor: https://reg.clinicalgenome.org/allele/ab/desc/GRCh38%20(chrX:p)add
+
+-  **Identifier**: CAAB267958021
+-  **Look up via identifier**: https://reg.clinicalgenome.org/allele/CAAB267958021
+-  **Look up via descriptor**: https://reg.clinicalgenome.org/allele/ab/desc/GRCh38%20(chrX:p)add
 </td>
 <td>
  <span dir="">Aneuploidy</span>