User:Plivdan

Diagnosis
Autosomal dominant or X-linked familial disorders often prompt prenatal testing for germline mosaicism. This diagnosis may involve minimally invasive procedures, such as blood sampling or amniotic fluid sampling. 2,4,5,6,8 Collected samples can be sequenced via common DNA testing methods, such as Sanger Sequencing, MLPA, or Southern Plot analysis, to look for variations on relevant genes connected to the disorder. 11,12