Chromosomal-Abnormalities.md

@@ -14,9 +14,9 @@
 <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>