These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 1071344)

  • 21. The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks.
    Janku P; Robinow M; Kelly T; Bralley R; Baynes A; Edgerton MT
    Am J Med Genet; 1980; 5(2):117-23. PubMed ID: 7395906
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Retrospective diagnoses of previously missed syndromic disorders among 1,000 patients with cleft lip, cleft palate, or both.
    Shprintzen RJ; Siegel-Sadewitz VL; Amato J; Goldberg RB
    Birth Defects Orig Artic Ser; 1985; 21(2):85-92. PubMed ID: 3840043
    [No Abstract]   [Full Text] [Related]  

  • 23. [Variable expression of lower lip fistulas in Van der Woude syndrome].
    Opitz C; Witkowski R; Tinschert S
    Mund Kiefer Gesichtschir; 2000 Jul; 4(4):222-7. PubMed ID: 10994321
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The penetrance and variable expression of the Van der Woude syndrome: implications for genetic counseling.
    Shprintzen RJ; Goldberg RB; Sidoti EJ
    Cleft Palate J; 1980 Jan; 17(1):52-7. PubMed ID: 6928118
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic analysis in families with van der Woude syndrome.
    Burdick AB; Bixler D; Puckett CL
    J Craniofac Genet Dev Biol; 1985; 5(2):181-208. PubMed ID: 4019732
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hay-Wells syndrome in a child with mutation in the TP73L gene.
    Garcia Bartels N; Neumann LM; Mleczko A; Rubach K; Peters H; Rossi R; Sterry W; Blume-Peytavi U
    J Dtsch Dermatol Ges; 2007 Oct; 5(10):919-23. PubMed ID: 17910675
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Congenital abnormalities in combination with lip-jaw-palate clefts].
    Nover HU; Machtens E; Quang KD
    Fortschr Kiefer Gesichtschir; 1986; 31():180-3. PubMed ID: 3460948
    [No Abstract]   [Full Text] [Related]  

  • 28. Intrafamilial variability of popliteal pterygium syndrome: a family description.
    Khan SN; Hufnagle KG; Pool R
    Cleft Palate J; 1986 Jul; 23(3):233-6. PubMed ID: 3460725
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cognitive dysfunction in adults with Van der Woude syndrome.
    Nopoulos P; Richman L; Andreasen N; Murray JC; Schutte B
    Genet Med; 2007 Apr; 9(4):213-8. PubMed ID: 17438385
    [TBL] [Abstract][Full Text] [Related]  

  • 30. van der Woude syndrome in two families in China.
    Burdick AB; Ma LA; Dai ZH; Gao NN
    J Craniofac Genet Dev Biol; 1987; 7(4):413-8. PubMed ID: 3429616
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing.
    Pengelly RJ; Upstill-Goddard R; Arias L; Martinez J; Gibson J; Knut M; Collins AL; Ennis S; Collins A; Briceno I
    Clin Genet; 2015 Nov; 88(5):441-9. PubMed ID: 25441681
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Van der Woude syndrome: report of two cases with supplementary findings.
    More CB; Varma S; Tailor M; Bhavsar K
    Indian J Dent Res; 2013; 24(3):387-9. PubMed ID: 24025891
    [TBL] [Abstract][Full Text] [Related]  

  • 33. What else to look for in a child born with a cleft of the lip and/or palate.
    Pashayan HM
    Cleft Palate J; 1983 Jan; 20(1):54-82. PubMed ID: 6572576
    [No Abstract]   [Full Text] [Related]  

  • 34. AEC syndrome caused by heterozygous mutation in the SAM domain of p63 gene.
    Tomková H; Fujimoto W; Uchida T; Macko J; Gaillyová R; Bucková H
    Eur J Dermatol; 2010; 20(3):411-3. PubMed ID: 20156774
    [No Abstract]   [Full Text] [Related]  

  • 35. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
    Item CB; Turhani D; Thurnher D; Yerit K; Sinko K; Wittwer G; Adeyemo WL; Frei K; Erginel-Unaltuna N; Watzinger F; Ewers R
    Int J Mol Med; 2005 Feb; 15(2):247-51. PubMed ID: 15647839
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Genetic analysis of two families with van der Woude's syndrome (lip pits, cleft palate, and cleft lip syndrome)].
    Burdick AB; Ma LA; Gao N; Dai ZH
    Yi Chuan Xue Bao; 1988; 15(5):396-400. PubMed ID: 3273683
    [No Abstract]   [Full Text] [Related]  

  • 37. [Van der Woude syndrome in combination with ring chromosome 18].
    Kalker U; Gabriel M; Jacobi G
    Monatsschr Kinderheilkd; 1988 Feb; 136(2):95-8. PubMed ID: 3367915
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome.
    Shotelersuk V; Srichomthong C; Yoshiura K; Niikawa N
    Int J Mol Med; 2003 Apr; 11(4):505-7. PubMed ID: 12632105
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Lower lip pits: van der woude or kabuki syndrome?
    David-Paloyo FP; Yang X; Lin JL; Wong FH; Wu-Chou YH; Lo LJ
    Cleft Palate Craniofac J; 2014 Nov; 51(6):729-34. PubMed ID: 24088119
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP; Moerman P
    Genet Couns; 1998; 9(1):61-2. PubMed ID: 9555592
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.