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 *

173 related articles for article (PubMed ID: 10417281)

  • 1. A locus for isolated cleft palate, located on human chromosome 2q32.
    Brewer CM; Leek JP; Green AJ; Holloway S; Bonthron DT; Markham AF; FitzPatrick DR
    Am J Hum Genet; 1999 Aug; 65(2):387-96. PubMed ID: 10417281
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of SATB2 as the cleft palate gene on 2q32-q33.
    FitzPatrick DR; Carr IM; McLaren L; Leek JP; Wightman P; Williamson K; Gautier P; McGill N; Hayward C; Firth H; Markham AF; Fantes JA; Bonthron DT
    Hum Mol Genet; 2003 Oct; 12(19):2491-501. PubMed ID: 12915443
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12).
    Machida J; Félix TM; Murray JC; Yoshiura K; Tanemura M; Kamamoto M; Shimozato K; Sonta S; Ono T
    Cleft Palate Craniofac J; 2009 Sep; 46(5):532-40. PubMed ID: 19929093
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.
    Urquhart J; Black GC; Clayton-Smith J
    Eur J Med Genet; 2009; 52(6):454-7. PubMed ID: 19576302
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Pierre Robin sequence and interstitial deletion 2q32.3-q33.2.
    Houdayer C; Portnoï MF; Vialard F; Soupre V; Crumière C; Taillemite JL; Couderc R; Vazquez MP; Bahuau M
    Am J Med Genet; 2001 Aug; 102(3):219-26. PubMed ID: 11484197
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
    Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
    Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.
    Van Buggenhout G; Van Ravenswaaij-Arts C; Mc Maas N; Thoelen R; Vogels A; Smeets D; Salden I; Matthijs G; Fryns JP; Vermeesch JR
    Eur J Med Genet; 2005; 48(3):276-89. PubMed ID: 16179223
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.
    Amasdl S; Natiq A; Sbiti A; Zerkaoui M; Lyahyai J; Amzazi S; Liehr T; Sefiani A
    BMC Res Notes; 2016 Jan; 9():5. PubMed ID: 26724919
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate.
    Sahoo T; Theisen A; Sanchez-Lara PA; Marble M; Schweitzer DN; Torchia BS; Lamb AN; Bejjani BA; Shaffer LG; Lacassie Y
    Am J Med Genet A; 2011 Jul; 155A(7):1646-53. PubMed ID: 21671386
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). Letter.
    Balci S; Aypar E; Engiz O
    Cleft Palate Craniofac J; 2010 Jul; 47(4):431-2. PubMed ID: 20163253
    [No Abstract]   [Full Text] [Related]  

  • 17. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
    Shetty S; Boycott KM; Gillan TL; Bowser K; Parboosingh JS; McInnes B; Chernos JE; Bernier FP
    Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Classification of oral clefts by affection site and laterality: a genotype-phenotype correlation study.
    Farina A; Wyszynski DF; Pezzetti F; Scapoli L; Martinelli M; Carinci F; Carls F; Nardelli GB; Tognon M; Carinci P
    Orthod Craniofac Res; 2002 Aug; 5(3):185-91. PubMed ID: 12194669
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
    Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
    Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability.
    Johansson S; Berland S; Gradek GA; Bongers E; de Leeuw N; Pfundt R; Fannemel M; Rødningen O; Brendehaug A; Haukanes BI; Hovland R; Helland G; Houge G
    Am J Med Genet A; 2014 Jul; 164A(7):1622-6. PubMed ID: 24678003
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.