BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 8494785)

  • 1. Transgenic mouse model of X-linked cleft palate.
    Wilson JB; Ferguson MW; Jenkins NA; Lock LF; Copeland NG; Levine AJ
    Cell Growth Differ; 1993 Feb; 4(2):67-76. PubMed ID: 8494785
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An X-linked recessive mutation producing cleft palate, crooked tail, and polydactyly in mice.
    Barra J
    J Hered; 1990; 81(5):388-92. PubMed ID: 2230077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
    Griffith AJ; Burgess DL; Kohrman DC; Yu J; Blaschak J; Blanton SH; Boehnke M; Hecht JT; Overhauser J; Meisler MH
    Genomics; 1996 Jun; 34(3):299-303. PubMed ID: 8786128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked cleft palate and ankyloglossia in an Icelandic family.
    Björnsson A; Arnason A; Tippet P
    Cleft Palate J; 1989 Jan; 26(1):3-8. PubMed ID: 2563678
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A postimplantation lethal mutation induced by transgene insertion on mouse chromosome 8.
    Pravtcheva DD; Wise TL
    Genomics; 1995 Dec; 30(3):529-44. PubMed ID: 8825640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.
    Stanier P; Forbes SA; Arnason A; Bjornsson A; Sveinbjornsdottir E; Williamson R; Moore G
    Genomics; 1993 Sep; 17(3):549-55. PubMed ID: 8244369
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked cleft palate.
    Bixler D
    Am J Med Genet; 1987 Oct; 28(2):503-5. PubMed ID: 3425624
    [No Abstract]   [Full Text] [Related]  

  • 8. The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models.
    Gritli-Linde A
    Curr Top Dev Biol; 2008; 84():37-138. PubMed ID: 19186243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.
    Culiat CT; Stubbs LJ; Woychik RP; Russell LB; Johnson DK; Rinchik EM
    Nat Genet; 1995 Nov; 11(3):344-6. PubMed ID: 7581464
    [TBL] [Abstract][Full Text] [Related]  

  • 10. exma: an X-linked insertional mutation that disrupts forebrain and eye development.
    Cunningham D; Xiao Q; Chatterjee A; Sulik K; Juriloff D; Elder F; Harrison W; Schuster G; Overbeek PA; Herman GE
    Mamm Genome; 2002 Apr; 13(4):179-85. PubMed ID: 11956759
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.
    Braybrook C; Warry G; Howell G; Arnason A; Bjornsson A; Moore GE; Ross MT; Stanier P
    Genomics; 2001 Mar; 72(2):128-36. PubMed ID: 11401425
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage of an X-chromosome cleft palate gene.
    Moore GE; Ivens A; Chambers J; Farrall M; Williamson R; Page DC; Bjornsson A; Arnason A; Jensson O
    Nature; 1987 Mar 5-11; 326(6108):91-2. PubMed ID: 2881212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE; Hamel BC; van Bokhoven H; de Jager F; van den Helm B; Kremer H; Heineman-de Boer JA; Ropers HH; Mariman EC
    Am J Med Genet; 1999 Jul; 85(3):216-20. PubMed ID: 10398231
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A further X-linked isolated nonsyndromic cleft palate family with a nonexpressing obligate affected male.
    Hall BD
    Am J Med Genet; 1987 Jan; 26(1):239-40. PubMed ID: 3812573
    [No Abstract]   [Full Text] [Related]  

  • 15. Transgenic mouse model of hemifacial microsomia: cloning and characterization of insertional mutation region on chromosome 10.
    Naora H; Kimura M; Otani H; Yokoyama M; Koizumi T; Katsuki M; Tanaka O
    Genomics; 1994 Oct; 23(3):515-9. PubMed ID: 7531669
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X-linked cleft palate gene.
    Bush JO; Lan Y; Maltby KM; Jiang R
    Dev Dyn; 2002 Nov; 225(3):322-6. PubMed ID: 12412015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.
    Dostal A; Nemeckova J; Gaillyova R
    J Craniomaxillofac Surg; 2009 Jul; 37(5):272-5. PubMed ID: 19157891
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
    Braybrook C; Doudney K; Marçano AC; Arnason A; Bjornsson A; Patton MA; Goodfellow PJ; Moore GE; Stanier P
    Nat Genet; 2001 Oct; 29(2):179-83. PubMed ID: 11559848
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA; Brennan L; Richardson M; Coffey A; Cole CG; Gregory SG; Bentley DR; Mumm S; Moore GE; Stanier P
    Genomics; 1996 Jan; 31(1):36-43. PubMed ID: 8808277
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.
    Candille SI; Pardue MT; McCall MA; Peachey NS; Gregg RG
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2748-51. PubMed ID: 10509675
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.