APA (7th ed.) Citation
(2026). A c.89G>C p.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith‐Lemli‐Opitz Syndrome. Molecular Genetics & Genomic Medicine.
Chicago Style (17th ed.) Citation
"A C.89G>C P.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith‐Lemli‐Opitz Syndrome." Molecular Genetics & Genomic Medicine 2026.
MLA (9th ed.) Citation
"A C.89G>C P.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith‐Lemli‐Opitz Syndrome." Molecular Genetics & Genomic Medicine, 2026.
Warning: These citations may not always be 100% accurate.