There are two different types of clefts, syndromic and non-syndromic. However, significant overlay between the two occur (Stanier and Moore, 1). The syndromic forms involve one or more phenotype changing, making it difficult to track and locate the exact gene, gene mutation, or other factor causing CL/P. Non-syndromic forms of CL/P occur in isolation from other phenotypes or abnormalities. Non-syndromic forms are the easiest to pin-point, and with the addition of approximately seventy percent of CL/P being non-syndromic, non-syndromic forms are the most commonly studied. They are the most studied because they promise a solution to the CL/P faster than finding syndromic forms. The different forms of CL/P result in a multitude of genes and their mutations needing to be studied. Some genes will cause a cleft lip, others a cleft palate and even some will cause