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vermilion defect相关文献:
Wiedemann-Steiner Syndrome.
Sheppard SE, Quintero-Rivera F.
2022 May 26. 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:35617449
Coffin-Siris Syndrome.
Schrier Vergano S, Santen G, Wieczorek D, Matsumoto N.
2013 Apr 4 [updated 2025 May 15]. 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:23556151
Management of an Upper Cutaneous and Vermilion Lip Defect.
Bailey AM, Jansen C, Zitelli JA, Hsia LB.
Dermatol Surg. 2023 Mar 1;49(3):287-289. doi: 10.1097/DSS.0000000000003522. Epub 2022 Jul 5.
PMID:36863039
Correlation of vermilion symmetry to alveolar cleft defect in unilateral cleft lip repair.
Bonanthaya K, Rao DD, Shetty P, Uguru C.
Int J Oral Maxillofac Surg. 2016 Jun;45(6):688-91. doi: 10.1016/j.ijom.2015.11.019. Epub 2016 Jan 2.
PMID:26754270
A novel technique of reconstruction of vermilion by pedicled myomucosal labial vestibular flap in traumatic defect of lower lip.
Sahai R, Singh S, Singh AK.
Natl J Maxillofac Surg. 2022 Jan-Apr;13(1):125-129. doi: 10.4103/njms.NJMS_197_20. Epub 2022 Mar 8.
PMID:35911806
Effective method for reconstruction of remaining lower lip vermilion defect after a mental V-Y advancement flap.
Kim JH, Ahn CH, Kim S, Lee WS, Oh SH.
Arch Craniofac Surg. 2019 Apr;20(2):76-83. doi: 10.7181/acfs.2018.01984. Epub 2019 Apr 20.
PMID:31048643
Fryns Syndrome.
Slavotinek A.
2007 Apr 18 [updated 2020 Sep 17]. 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:20301632
Aspartylglucosaminuria.
Goodspeed K, Chen X, Tchan M.
2024 Jan 18. 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:38252773
Char Syndrome.
Gelb BD.
2003 Aug 15 [updated 2020 May 21]. 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:20301285
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum.
Yates TM, Drucker M, Barnicoat A, Low K, Gerkes EH, Fry AE, Parker MJ, O'Driscoll M, Charles P, Cox H, Marey I, Keren B, Rinne T, McEntagart M, Ramachandran V, Drury S, Vansenne F, Sival DA, Herkert JC, Callewaert B, Tan WH, Balasubramanian M.
Hum Mutat. 2020 May;41(5):1042-1050. doi: 10.1002/humu.24001. Epub 2020 Mar 5.
PMID:32097528
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