APA (7th ed.) Citation

Zufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, Yoav Zehavi, Morad Khayat, Haneen Jabaly-Habib, . . . Ronen Spiegel. (2022). A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay. Frontiers Media S.A..

Chicago Style (17th ed.) Citation

Zufit Hexner-Erlichman, et al. A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay. Frontiers Media S.A., 2022.

MLA (9th ed.) Citation

Zufit Hexner-Erlichman, et al. A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay. Frontiers Media S.A., 2022.