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congenital velopharyngeal incompetence相关文献:
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.
PMID:20301696
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.
PMID:29023086
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.
PMID:28333430
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.
PMID:31145570
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.
PMID:37869607
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.
PMID:33105231
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.
PMID:25989227
Evidence-Based Medicine: Cleft Palate.
Woo AS.
Plast Reconstr Surg. 2017 Jan;139(1):191e-203e. doi: 10.1097/PRS.0000000000002854.
PMID:28027255
Acquired Velopharyngeal Dysfunction: Survey, Literature Review, and Clinical Recommendations.
Guyton KB, Sandage MJ, Bailey D, Haak N, Molt L, Plumb A.
Am J Speech Lang Pathol. 2018 Nov 21;27(4):1572-1597. doi: 10.1044/2018_AJSLP-17-0222.
PMID:30208483
CATCH 22.
Hall JG.
J Med Genet. 1993 Oct;30(10):801-2. doi: 10.1136/jmg.30.10.801.
PMID:8230153
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