BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 18204864)

  • 1. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.
    Jalali A; Aldinger KA; Chary A; McLone DG; Bowman RM; Le LC; Jardine P; Newbury-Ecob R; Mallick A; Jafari N; Russell EJ; Curran J; Nguyen P; Ouahchi K; Lee C; Dobyns WB; Millen KJ; Pina-Neto JM; Kessler JA; Bassuk AG
    Hum Genet; 2008 Apr; 123(3):237-45. PubMed ID: 18204864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypes.
    McNiven V; Ito YA; Hartley T; Kernohan K; Miller E; ; Armour CM
    Am J Med Genet A; 2019 May; 179(5):837-841. PubMed ID: 30773799
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generations.
    Dietvorst S; Devriendt K; Lambert J; Boogaerts A; Van Den Bogaert K; Buyse G; Van Calenbergh F
    Eur J Med Genet; 2023 Apr; 66(4):104713. PubMed ID: 36702440
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
    Paterson AD; Liu XQ; Wang K; Magistroni R; Song X; Kappel J; Klassen J; Cattran D; St George-Hyslop P; Pei Y
    J Am Soc Nephrol; 2007 Aug; 18(8):2408-15. PubMed ID: 17634434
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
    Hocking LJ; Herbert CA; Nicholls RK; Williams F; Bennett ST; Cundy T; Nicholson GC; Wuyts W; Van Hul W; Ralston SH
    Am J Hum Genet; 2001 Nov; 69(5):1055-61. PubMed ID: 11555792
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles.
    Darbro BW; Mahajan VB; Gakhar L; Skeie JM; Campbell E; Wu S; Bing X; Millen KJ; Dobyns WB; Kessler JA; Jalali A; Cremer J; Segre A; Manak JR; Aldinger KA; Suzuki S; Natsume N; Ono M; Hai HD; Viet le T; Loddo S; Valente EM; Bernardini L; Ghonge N; Ferguson PJ; Bassuk AG
    Hum Mutat; 2013 Aug; 34(8):1075-9. PubMed ID: 23674478
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dandy-Walker malformation in the Meckel syndrome.
    Summers MC; Donnenfeld AE
    Am J Med Genet; 1995 Jan; 55(1):57-61. PubMed ID: 7702098
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
    Jiao X; Ritter R; Hejtmancik JF; Edwards AO
    Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4498-503. PubMed ID: 15557460
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dandy-Walker syndrome together with occipital encephalocele.
    Cakmak A; Zeyrek D; Cekin A; Karazeybek H
    Minerva Pediatr; 2008 Aug; 60(4):465-8. PubMed ID: 18511899
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal dominant occipital cephalocele.
    Bassuk AG; McLone D; Bowman R; Kessler JA
    Neurology; 2004 May; 62(10):1888-90. PubMed ID: 15159504
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial occurrence of atretic cephaloceles.
    Martínez-Lage JF; Martínez Robledo A; Poza M; Sola J
    Pediatr Neurosurg; 1996 Nov; 25(5):260-4. PubMed ID: 9309791
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dandy-Walker malformation in the Meckel syndrome.
    Herriot R; Hallam LA; Gray ES
    Am J Med Genet; 1991 May; 39(2):207-10. PubMed ID: 2063927
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.
    Cormand B; Pihko H; Bayés M; Valanne L; Santavuori P; Talim B; Gershoni-Baruch R; Ahmad A; van Bokhoven H; Brunner HG; Voit T; Topaloglu H; Dobyns WB; Lehesjoki AE
    Neurology; 2001 Apr; 56(8):1059-69. PubMed ID: 11320179
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Occipital encephalocele associated with Dandy-Walker malformation: a case-based review.
    Gutierrez F; Ballestero M; Herrera D; Gonzalez C; Cardona A; Mora L
    Childs Nerv Syst; 2022 Sep; 38(9):1683-1688. PubMed ID: 35588332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of chromosome 2q36.1-36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families.
    Gu J; Huang J; Li C; Zhao L; Huang F; Liao Z; Li T; Wei Q; Lin Z; Pan Y; Huang J; Wang X; Lin Q; Lu C; Wu Y; Cao S; Wu J; Xu H; Yu B; Shen Y
    J Med Genet; 2009 Oct; 46(10):657-62. PubMed ID: 19416804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.
    Ammar M; Bouchlaka-Souissi C; Helms CA; Zaraa I; Jordan CT; Anbunathan H; Bouhaha R; Kouidhi S; Doss N; Dhaoui R; Ben Osman A; Ben Ammar El Gaied A; Marrakchi R; Mokni M; Bowcock AM
    Br J Dermatol; 2013 Mar; 168(3):583-7. PubMed ID: 23013406
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 2p14 is linked to susceptibility to leprosy.
    Yang Q; Liu H; Low HQ; Wang H; Yu Y; Fu X; Yu G; Chen M; Yan X; Chen S; Huang W; Liu J; Zhang F
    PLoS One; 2012; 7(1):e29747. PubMed ID: 22238647
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
    Lucas GJ; Riches PL; Hocking LJ; Cundy T; Nicholson GC; Walsh JP; Ralston SH
    J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation.
    Lefort G; Blanchet P; Chaze AM; Girardet A; Sarda P; Demaille J; Pellestor F
    J Med Genet; 2001 Jan; 38(1):67-73. PubMed ID: 11334011
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.