22q11.2 Deletion Syndrome.
McDonald-McGinn DM, Hain HS, Emanuel BS, Zackai EH.
1999 Sep 23 [updated 2025 May 8]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
SATB2-Associated Syndrome.
Zarate YA, Bosanko K, Fish J.
2017 Oct 12 [updated 2024 Jun 20]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
KCNK9 Imprinting Syndrome.
Zadeh N, Graham JM Jr.
2017 Mar 23. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
Apert Syndrome.
Wenger TL, Hing AV, Evans KN.
2019 May 30. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
Congenital velopharyngeal incompetence in Kabuki make-up syndrome.
Lan K, Michiwaki Y, Sunaga S, Michi K.
Int J Oral Maxillofac Surg. 1995 Aug;24(4):298-300. doi: 10.1016/s0901-5027(95)80033-6.
CATCH 22.
Hall JG.
J Med Genet. 1993 Oct;30(10):801-2. doi: 10.1136/jmg.30.10.801.
Management of submucous cleft palate.
Dean KM, Leeper LK.
Curr Opin Otolaryngol Head Neck Surg. 2020 Dec;28(6):410-413. doi: 10.1097/MOO.0000000000000673.
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).
Allen NM, O'Rahelly M, Eymard B, Chouchane M, Hahn A, Kearns G, Kim DS, Byun SY, Nguyen CE, Schara-Schmidt U, Kölbel H, Marina AD, Schneider-Gold C, Roefke K, Thieme A, Van den Bergh P, Avalos G, Álvarez-Velasco R, Natera-de Benito D, Cheng MHM, Chan WK, Wan HS, Thomas MA, Borch L, Lauzon J, Kornblum C, Reimann J, Mueller A, Kuntzer T, Norwood F, Ramdas S, Jacobson LW, Jie X, Fernandez-Garcia MA, Wraige E, Lim M, Lin JP, Claeys KG, Aktas S, Oskoui M, Hacohen Y, Masud A, Leite MI, Palace J, De Vivo D, Vincent A, Jungbluth H.
Brain. 2023 Oct 3;146(10):4233-4246. doi: 10.1093/brain/awad153.
Editorial: Congenital craniofacial deformities: genetic and clinical aspects.
Huang H, Du J.
Front Oral Health. 2023 Oct 5;4:1298447. doi: 10.3389/froh.2023.1298447. eCollection 2023.
[Velopharyngeal closure pattern and speech characteristics of patients congenital velopharyngeal insufficiency].
Wang X, Guo CL, Shi B, Yin H.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2020 Dec 1;38(6):662-666. doi: 10.7518/hxkq.2020.06.010.
