BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 16284940)

  • 41. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
    Al Ageeli E; Drunat S; Delanoë C; Perrin L; Baumann C; Capri Y; Fabre-Teste J; Aboura A; Dupont C; Auvin S; El Khattabi L; Chantereau D; Moncla A; Tabet AC; Verloes A
    Eur J Med Genet; 2014 Jan; 57(1):5-14. PubMed ID: 24239951
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
    Wang JC; Vaccarello-Cruz M; Ross L; Owen R; Pratt VM; Lightman K; Liu Y; Hafezi K; Cherif D; Sahoo T
    Am J Med Genet A; 2013 Jul; 161A(7):1695-701. PubMed ID: 23686718
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Sequence-based, in situ detection of chromosomal abnormalities at high resolution.
    Knoll JH; Rogan PK
    Am J Med Genet A; 2003 Sep; 121A(3):245-57. PubMed ID: 12923866
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
    Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization.
    Yokoyama-Rebollar E; Ruiz-Herrera A; Lieberman-Hernández E; Del Castillo-Ruiz V; Sánchez-Sandoval S; Ávila-Flores SM; Castrillo JL
    Mol Cytogenet; 2015; 8():27. PubMed ID: 25901183
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Erdel M; Schuffenhauer S; Buchholz B; Barth-Witte U; Köchl S; Utermann B; Duba HC; Utermann G
    Hum Genet; 1996 Jun; 97(6):784-93. PubMed ID: 8641697
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
    Kuwano A; Mutirangura A; Dittrich B; Buiting K; Horsthemke B; Saitoh S; Niikawa N; Ledbetter SA; Greenberg F; Chinault AC
    Hum Mol Genet; 1992 Sep; 1(6):417-25. PubMed ID: 1363801
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.
    Thomas NS; Browne CE; Oley C; Healey S; Crolla JA
    Hum Genet; 1999 Nov; 105(5):384-7. PubMed ID: 10598802
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.
    Kuroda Y; Ohashi I; Saito T; Nagai J; Ida K; Naruto T; Wada T; Kurosawa K
    Am J Med Genet A; 2014 Nov; 164A(11):2873-8. PubMed ID: 25099823
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC; Lopes GM; Koiffmann CP
    Ann Genet; 2004; 47(3):267-73. PubMed ID: 15337472
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
    Hartin SN; Hossain WA; Weisensel N; Butler MG
    Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genomic imprinting and human chromosome 15.
    Repetto GM
    Biol Res; 2001; 34(2):141-5. PubMed ID: 11715207
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
    Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
    Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report.
    Han JY; Lee HJ; Lee YM; Park J
    Children (Basel); 2021 Apr; 8(4):. PubMed ID: 33924158
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
    Buiting K; Dittrich B; Gross S; Lich C; Färber C; Buchholz T; Smith E; Reis A; Bürger J; Nöthen MM; Barth-Witte U; Janssen B; Abeliovich D; Lerer I; van den Ouweland AM; Halley DJ; Schrander-Stumpel C; Smeets H; Meinecke P; Malcolm S; Gardner A; Lalande M; Nicholls RD; Friend K; Schulze A; Matthijs G; Kokkonen H; Hilbert P; Van Maldergem L; Glover G; Carbonell P; Willems P; Gillessen-Kaesbach G; Horsthemke B
    Am J Hum Genet; 1998 Jul; 63(1):170-80. PubMed ID: 9634532
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Mechanisms of imprinting of the Prader-Willi/Angelman region.
    Horsthemke B; Wagstaff J
    Am J Med Genet A; 2008 Aug; 146A(16):2041-52. PubMed ID: 18627066
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
    Christian SL; Brune CW; Sudi J; Kumar RA; Liu S; Karamohamed S; Badner JA; Matsui S; Conroy J; McQuaid D; Gergel J; Hatchwell E; Gilliam TC; Gershon ES; Nowak NJ; Dobyns WB; Cook EH
    Biol Psychiatry; 2008 Jun; 63(12):1111-7. PubMed ID: 18374305
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.