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 *

240 related articles for article (PubMed ID: 7711723)

  • 1. Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region.
    Davies AF; Stephens RJ; Olavesen MG; Heather L; Dixon MJ; Magee A; Flinter F; Ragoussis J
    Hum Mol Genet; 1995 Jan; 4(1):121-8. PubMed ID: 7711723
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3.
    Donnai D; Heather LJ; Sinclair P; Thakker Y; Scambler PJ; Dixon MJ
    Clin Dysmorphol; 1992 Apr; 1(2):89-97. PubMed ID: 1345518
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.
    Davies AF; Imaizumi K; Mirza G; Stephens RS; Kuroki Y; Matsuno M; Ragoussis J
    J Med Genet; 1998 Oct; 35(10):857-61. PubMed ID: 9783713
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate.
    Yoshiura K; Machida J; Daack-Hirsch S; Patil SR; Ashworth LK; Hecht JT; Murray JC
    Genomics; 1998 Dec; 54(2):231-40. PubMed ID: 9828125
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
    Schutte BC; Bjork BC; Coppage KB; Malik MI; Gregory SG; Scott DJ; Brentzell LM; Watanabe Y; Dixon MJ; Murray JC
    Genome Res; 2000 Jan; 10(1):81-94. PubMed ID: 10645953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting.
    Ross AP; Mansilla MA; Choe Y; Helminski S; Sturm R; Maute RL; May SR; Hozyasz KK; Wójcicki P; Mostowska A; Davidson B; Adamopoulos IE; Pleasure SJ; Murray JC; Zarbalis KS
    PLoS One; 2013; 8(7):e69333. PubMed ID: 23935987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Toward an orofacial gene regulatory network.
    Kousa YA; Schutte BC
    Dev Dyn; 2016 Mar; 245(3):220-32. PubMed ID: 26332872
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
    Schutte BC; Sander A; Malik M; Murray JC
    Genomics; 1996 Sep; 36(3):507-14. PubMed ID: 8884274
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21.
    Ounap K; Ilus T; Laidre P; Uibo O; Tammur P; Bartsch O
    Am J Med Genet A; 2005 Sep; 137A(3):323-7. PubMed ID: 16094674
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H; Wong FK; Rautio J; Ollikainen V; Karsten A; Larson O; Teh BT; Huggare J; Lahermo P; Larsson C; Kere J
    Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.
    Chen CP; Tzen CY; Chern SR; Tsai FJ; Hsu CY; Lee CC; Lee MS; Pan CW; Wang W
    Eur J Med Genet; 2009; 52(1):59-61. PubMed ID: 19049908
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region.
    Davies SJ; Wise C; Venkatesh B; Mirza G; Jefferson A; Volpi EV; Ragoussis J
    Cytogenet Genome Res; 2004; 105(1):47-53. PubMed ID: 15218257
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].
    Doray B; Badila-Timbolschi D; Schaefer E; Fattori D; Monga B; Dott B; Favre R; Kohler M; Nisand I; Viville B; Kauffmann I; Bruant-Rodier C; Grollemund B; Rinkenbach R; Astruc D; Gasser B; Lindner V; Marcellin L; Flori E; Girard-Lemaire F; Dollfus H
    Arch Pediatr; 2012 Oct; 19(10):1021-9. PubMed ID: 22925539
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 20856054
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microdeletion of chromosome 15q24.3-25.2 and orofacial clefting.
    Sing B; Song D; DeSandre G; Govindaswami B; Rosenthal S; Gunn S; Wallerstein R
    Cleft Palate Craniofac J; 2011 Sep; 48(5):596-600. PubMed ID: 20518684
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
    Charzewska A; Obersztyn E; Hoffman-Zacharska D; Lenart J; Poznański J; Bal J
    Cleft Palate Craniofac J; 2015 Sep; 52(5):e161-7. PubMed ID: 25489771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A.
    Hecht JT; Wang Y; Connor B; Blanton SH; Daiger SP
    Am J Hum Genet; 1993 Jun; 52(6):1230-3. PubMed ID: 8099257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M; Schinzel A
    Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6.
    Eiberg H; Bixler D; Nielsen LS; Conneally PM; Mohr J
    Clin Genet; 1987 Aug; 32(2):129-32. PubMed ID: 2888553
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.
    Sander A; Schmelzle R; Murray J
    Hum Mol Genet; 1994 Apr; 3(4):575-8. PubMed ID: 8069301
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.