Chromosomal-Abnormalities.md

@@ -88,25 +88,26 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chr21:q10)::(chr14:q10) - \[Down syndrome, unbalanced thus partial trisomy 21\] GRCh38 (chr21:q)::(chr14:q10),(chr21)del,(chr14)del - \[Variant for balanced carrier\]</span>
+* <span dir="">GRCh38 (chr21:q10)::(chr14:q10)</span>
+* <span dir="">GRCh38 (chr21:q)::(chr14:q10),(chr21)del,(chr14)del </span>
 </td>
 <td>
 
 <span dir="">Aneuploidy</span>
 </td>
-<td>
-
-</td>
+<td>GRCh38 (chr21:q10)::(chr14:q10) - \[Down syndrome, unbalanced thus partial trisomy 21\] GRCh38 (chr21:q)::(chr14:q10),(chr21)del,(chr14)del - \[Variant for balanced carrier\]</td>
 </tr>
 <tr>
 <td>Fragile X syndrome</td>
 <td>
 
-<span dir="">GRCh38 (chrX:147912050-147912052)x201 - \[ClinVar sentinal for "200+" repeats variant, likely pathogenic\]<br>GRCh38 (chrX:147912050-147912052)x201,500 - \[generalized CNV for "all" likely pathogenic variants resulting in fragile X\]</span>
+* <span dir="">GRCh38 (chrX:147912050-147912052)x201 </span>
+* <span dir="">GRCh38 (chrX:147912050-147912052)x201,500 </span>
 </td>
 <td>Poly Nucleotide Repeat</td>
 <td>
 
+GRCh38 (chrX:147912050-147912052)x201 - \[ClinVar sentinal for "200+" repeats variant, likely pathogenic\]<br>GRCh38 (chrX:147912050-147912052)x201,500 - \[generalized CNV for "all" likely pathogenic variants resulting in fragile X\]
 </td>
 </tr>
 <tr>
@@ -118,7 +119,7 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chrX:q10)::(chrX:q10),(chrX:p)del </span>
+<span dir="">GRCh38 (chrX:q10)::(chrX:q10),(chrX:p)del</span>
 </td>
 <td>Other - Isochromosome</td>
 <td>- \[form of Turner syndrome, p-arm loss of chrX\]</td>
@@ -132,7 +133,7 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chr14:p)::(chr14:q) </span>
+<span dir="">GRCh38 (chr14:p)::(chr14:q)</span>
 </td>
 <td>Other - Ring chromosome</td>
 <td>\[associated with epilepsy and mental retardation\]</td>