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Results: 20

Select item 230377841.

An alternative technique using a gutta percha points and blue methylene to excision of congenital fistula of lower lip in patient with Van der Woude syndrome.

Castro CH, De Carvalho MF, Veloso DC, De Moraes M.

Stomatologija. 2012;14(2):60-4.

PMID:: 23037784; [PubMed - indexed for MEDLINE]

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Select item 228011582.

Early release of interalveolar synechiae under general anesthesia through fiberscopic nasal intubation.

Svee A, Frykholm P, Linder A, Hakelius M, Skoog V, Nowinski D.

J Craniofac Surg. 2012 Jul;23(4):e299-302. doi: 10.1097/SCS.0b013e318252f314.

PMID:: 22801158; [PubMed - indexed for MEDLINE]

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Select item 224405373.

Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: review of the literature.

Salahshourifar I, Wan Sulaiman WA, Halim AS, Zilfalil BA.

Eur J Med Genet. 2012 Jun;55(6-7):389-93. doi: 10.1016/j.ejmg.2012.02.006. Epub 2012 Mar 3. Review.

PMID:: 22440537; [PubMed - indexed for MEDLINE]

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Select item 219994504.

Symmetric lower lip pits - Van Der Woude syndrome.

Shah V, Krasemann T.

J Paediatr Child Health. 2011 Oct;47(10):757. doi: 10.1111/j.1440-1754.2011.02193.x. No abstract available.

PMID:: 21999450; [PubMed - indexed for MEDLINE]

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Select item 219594205.

Genetics of syndromic and nonsyndromic cleft lip and palate.

Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S.

J Craniofac Surg. 2011 Sep;22(5):1722-6. doi: 10.1097/SCS.0b013e31822e5e4d. Review.

PMID:: 21959420; [PubMed - indexed for MEDLINE]

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Select item 219577926.

Oral and maxillofacial pathology. Case of the month. Van der Woude syndrome (VWS).

Vigneswaran N, Demian N.

Tex Dent J. 2011 Aug;128(8):768, 772-3. No abstract available.

PMID:: 21957792; [PubMed - indexed for MEDLINE]

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Select item 219119867.

Pattern of craniofacial anomalies seen in a tertiary care hospital in Saudi Arabia.

Aziza A, Kandasamy R, Shazia S.

Ann Saudi Med. 2011 Sep-Oct;31(5):488-93. doi: 10.4103/0256-4947.84626.

PMID:: 21911986; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 217395758.

Monozygotic twins with variable expression of Van der Woude syndrome.

Jobling R, Ferrier RA, McLeod R, Petrin AL, Murray JC, Thomas MA.

Am J Med Genet A. 2011 Aug;155A(8):2008-10. doi: 10.1002/ajmg.a.34022. Epub 2011 Jul 7. No abstract available.

PMID:: 21739575; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 215742449.

Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.

Rorick NK, Kinoshita A, Weirather JL, Peyrard-Janvid M, de Lima RL, Dunnwald M, Shanske AL, Moretti-Ferreira D, Koillinen H, Kere J, Mansilla MA, Murray JC, Goudy SL, Schutte BC.

Am J Med Genet A. 2011 Jun;155A(6):1314-21. doi: 10.1002/ajmg.a.33980. Epub 2011 May 13.

PMID:: 21574244; [PubMed - indexed for MEDLINE]

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Select item 2152569810.

Van der Woude syndrome with an unusual intraoral finding.

Sarode GS, Desai RS, Sarode SC, Kulkarni MA.

Indian J Dent Res. 2011 Jan-Feb;22(1):164-5. doi: 10.4103/0970-9290.79988.

PMID:: 21525698; [PubMed - indexed for MEDLINE]

Free Article

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Select item 2146855711.

Novel IRF6 mutations in Honduran Van der Woude syndrome patients.

Birkeland AC, Larrabee Y, Kent DT, Flores C, Su GH, Lee JH, Haddad J Jr.

Mol Med Rep. 2011 Mar-Apr;4(2):237-41. doi: 10.3892/mmr.2011.423. Epub 2011 Jan 11.

PMID:: 21468557; [PubMed - indexed for MEDLINE]

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Select item 2144794212.

De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features.

Salahshourifar I, Halim AS, Sulaiman WA, Ariffin R, Naili Muhamad Nor N, Zilfalil BA.

Cytogenet Genome Res. 2011;134(2):83-7. doi: 10.1159/000325541. Epub 2011 Mar 25.

PMID:: 21447942; [PubMed - indexed for MEDLINE]

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Select item 2108265413.

IRF6 mutations in mixed isolated familial clefting.

Rutledge KD, Barger C, Grant JH, Robin NH.

Am J Med Genet A. 2010 Dec;152A(12):3107-9. doi: 10.1002/ajmg.a.33053.

PMID:: 21082654; [PubMed - indexed for MEDLINE]

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Select item 2085607314.

Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.

Scioletti AP, Brancati F, Gatta V, Antonucci I, Peissel B, Pizzuti A, Mortellaro C, Tetè S, Gherlone E, Palka G, Stuppia L.

J Craniofac Surg. 2010 Sep;21(5):1654-6. doi: 10.1097/SCS.0b013e3181ef69ef.

PMID:: 20856073; [PubMed - indexed for MEDLINE]

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Select item 2085605415.

Use of array comparative genome hybridization in orofacial clefting.

Gallego CJ, Grant J, Mikhail FM, Barger C, Robin NH.

J Craniofac Surg. 2010 Sep;21(5):1591-4. doi: 10.1097/SCS.0b013e3181ebcc9c.

PMID:: 20856054; [PubMed - indexed for MEDLINE]

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Select item 2085602016.

Wound complications after cleft repair in children with Van der Woude syndrome.

Jones JL, Canady JW, Brookes JT, Wehby GL, L'Heureux J, Schutte BC, Murray JC, Dunnwald M.

J Craniofac Surg. 2010 Sep;21(5):1350-3. doi: 10.1097/SCS.0b013e3181ec6aad.

PMID:: 20856020; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2084504717.

IRF6 mutations may not be a major cause of Van der Woude syndrome in India.

Moghe GA, Mauli S.

Eur J Pediatr. 2011 Jan;170(1):129. doi: 10.1007/s00431-010-1288-2. Epub 2010 Sep 16. No abstract available.

PMID:: 20845047; [PubMed - indexed for MEDLINE]

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Select item 2081824718.

Lower lip pits in a patient with van der Woude syndrome.

Baghestani S, Sadeghi N, Yavarian M, Alghasi H.

J Craniofac Surg. 2010 Sep;21(5):1380-1. doi: 10.1097/SCS.0b013e3181edc528.

PMID:: 20818247; [PubMed - indexed for MEDLINE]

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Select item 2080364319.

Two missense mutations of the IRF6 gene in two Japanese families with popliteal pterygium syndrome.

Matsuzawa N, Kondo S, Shimozato K, Nagao T, Nakano M, Tsuda M, Hirano A, Niikawa N, Yoshiura K.

Am J Med Genet A. 2010 Sep;152A(9):2262-7. doi: 10.1002/ajmg.a.33338.

PMID:: 20803643; [PubMed - indexed for MEDLINE]

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Select item 2018462020.

Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan.

Malik S, Kakar N, Hasnain S, Ahmad J, Wilcox ER, Naz S.

Clin Genet. 2010 Sep;78(3):247-56. doi: 10.1111/j.1399-0004.2010.01375.x. Epub 2010 Feb 10.

PMID:: 20184620; [PubMed - indexed for MEDLINE]

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3 free full-text articles in PubMed Central

Pattern of craniofacial anomalies seen in a tertiary care hospital in Saudi Arabia. [Ann Saudi Med. 2011]
Pattern of craniofacial anomalies seen in a tertiary care hospital in Saudi Arabia.
Aziza A, Kandasamy R, Shazia S. Ann Saudi Med. 2011 Sep-Oct; 31(5):488-93.
Monozygotic twins with variable expression of Van der Woude syndrome. [Am J Med Genet A. 2011]
Monozygotic twins with variable expression of Van der Woude syndrome.
Jobling R, Ferrier RA, McLeod R, Petrin AL, Murray JC, Thomas MA. Am J Med Genet A. 2011 Aug; 155A(8):2008-10. Epub 2011 Jul 7.
Wound complications after cleft repair in children with Van der Woude syndrome. [J Craniofac Surg. 2010]
Wound complications after cleft repair in children with Van der Woude syndrome.
Jones JL, Canady JW, Brookes JT, Wehby GL, L'Heureux J, Schutte BC, Murray JC, Dunnwald M. J Craniofac Surg. 2010 Sep; 21(5):1350-3.

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