Basha, M. (2018). Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes. BMJ Publishing Group.
Chicago Style (17th ed.) CitationBasha, M. Whole Exome Sequencing Identifies Mutations in 10% of Patients with Familial Non-syndromic Cleft Lip And/or Palate in Genes Mutated in Well-known Syndromes. BMJ Publishing Group, 2018.
MLA (9th ed.) CitationBasha, M. Whole Exome Sequencing Identifies Mutations in 10% of Patients with Familial Non-syndromic Cleft Lip And/or Palate in Genes Mutated in Well-known Syndromes. BMJ Publishing Group, 2018.
Warning: These citations may not always be 100% accurate.