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 *

197 related articles for article (PubMed ID: 8094063)

  • 21. Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
    Greger V; Knoll JH; Wagstaff J; Woolf E; Lieske P; Glatt H; Benn PA; Rosengren SS; Lalande M
    Am J Hum Genet; 1997 Mar; 60(3):574-80. PubMed ID: 9042916
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Angelman syndrome: validation of molecular cytogenetic analysis of chromosome 15q11-q13 for deletion detection.
    White L; Knoll JH
    Am J Med Genet; 1995 Mar; 56(1):101-5. PubMed ID: 7747771
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions.
    Gimelli G; Pujana MA; Patricelli MG; Russo S; Giardino D; Larizza L; Cheung J; Armengol L; Schinzel A; Estivill X; Zuffardi O
    Hum Mol Genet; 2003 Apr; 12(8):849-58. PubMed ID: 12668608
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.
    Nicholls RD; Pai GS; Gottlieb W; Cantú ES
    Ann Neurol; 1992 Oct; 32(4):512-8. PubMed ID: 1360787
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.
    Jiang YH; Pan Y; Zhu L; Landa L; Yoo J; Spencer C; Lorenzo I; Brilliant M; Noebels J; Beaudet AL
    PLoS One; 2010 Aug; 5(8):e12278. PubMed ID: 20808828
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
    Nicholls RD
    Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
    Buiting K; Gross S; Ji Y; Senger G; Nicholls RD; Horsthemke B
    Cytogenet Cell Genet; 1998; 81(3-4):247-53. PubMed ID: 9730612
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.
    Repetto GM; White LM; Bader PJ; Johnson D; Knoll JH
    Am J Med Genet; 1998 Sep; 79(2):82-9. PubMed ID: 9741464
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The mechanisms involved in formation of deletions and duplications of 15q11-q13.
    Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA
    J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The GABAA receptor beta 3-subunit gene (GABRB3) as a candidate responsible for central nerve disturbances in Angelman syndrome (AS)].
    Saitoh S; Niikawa N
    Nihon Rinsho; 1993 Sep; 51(9):2409-13. PubMed ID: 8411721
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kb.
    Buxton JL; Chan CT; Gilbert H; Clayton-Smith J; Burn J; Pembrey M; Malcolm S
    Hum Mol Genet; 1994 Aug; 3(8):1409-13. PubMed ID: 7987324
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.
    Greger V; Woolf E; Lalande M
    Hum Mol Genet; 1993 Jul; 2(7):921-4. PubMed ID: 8364575
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.
    Wagstaff J; Knoll JH; Glatt KA; Shugart YY; Sommer A; Lalande M
    Nat Genet; 1992 Jul; 1(4):291-4. PubMed ID: 1338769
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel patterns of inheritance of genetic disease are illustrated by the Angelman syndrome.
    Deng ZM; Woodage T; Smart R; Smith A; Trent RJ
    Med J Aust; 1993 Jun; 158(12):813-6. PubMed ID: 8326891
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome.
    Clayton-Smith J; Webb T; Robb SA; Dijkstra I; Willems P; Lam S; Cheng XJ; Pembrey ME; Malcolm S
    Am J Med Genet; 1992 Sep; 44(2):256-60. PubMed ID: 1360768
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Angelman syndrome in Denmark. birth incidence, genetic findings, and age at diagnosis.
    Mertz LG; Christensen R; Vogel I; Hertz JM; Nielsen KB; Grønskov K; Østergaard JR
    Am J Med Genet A; 2013 Sep; 161A(9):2197-203. PubMed ID: 23913711
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cytogenetic and molecular analysis in Angelman syndrome.
    Zackowski JL; Nicholls RD; Gray BA; Bent-Williams A; Gottlieb W; Harris PJ; Waters MF; Driscoll DJ; Zori RT; Williams CA
    Am J Med Genet; 1993 Apr; 46(1):7-11. PubMed ID: 8098583
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.
    Michaelis RC; Skinner SA; Lethco BA; Simensen RJ; Donlon TA; Tarleton J; Phelan MC
    Am J Med Genet; 1995 Jan; 55(1):120-6. PubMed ID: 7702085
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
    Nurmi EL; Bradford Y; Chen Y; Hall J; Arnone B; Gardiner MB; Hutcheson HB; Gilbert JR; Pericak-Vance MA; Copeland-Yates SA; Michaelis RC; Wassink TH; Santangelo SL; Sheffield VC; Piven J; Folstein SE; Haines JL; Sutcliffe JS
    Genomics; 2001 Sep; 77(1-2):105-13. PubMed ID: 11543639
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.