22q11.2 Deletion Syndrome.
McDonald-McGinn DM, Hain HS, Emanuel BS, Zackai EH.
1999 Sep 23 [updated 2025 May 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
SATB2-Associated Syndrome.
Zarate YA, Bosanko K, Fish J.
2017 Oct 12 [updated 2024 Jun 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
KCNK9 Imprinting Syndrome.
Zadeh N, Graham JM Jr.
2017 Mar 23. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
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.
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.
Apert Syndrome.
Wenger TL, Hing AV, Evans KN.
2019 May 30. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
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.
[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.
CATCH 22.
Hall JG.
J Med Genet. 1993 Oct;30(10):801-2. doi: 10.1136/jmg.30.10.801.
Developmental trajectories in 22q11.2 deletion.
Swillen A, McDonald-McGinn D.
Am J Med Genet C Semin Med Genet. 2015 Jun;169(2):172-81. doi: 10.1002/ajmg.c.31435. Epub 2015 May 18.
