BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

567 related articles for article (PubMed ID: 19159549)

  • 1. [Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].
    Li MR; Wang XZ; Liu XY; Yang YL; Bao XH; Zhang YH; Xiong H; Zhong N; Qin J; Wu XR; Pan H
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3257-61. PubMed ID: 19159549
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
    Procter M; Chou LS; Tang W; Jama M; Mao R
    Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
    Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Value of methylation-specific mutiplex ligation-dependent probe in the diagnosis of Prader-Willi syndrome].
    Zhan SN; Wang CZ; Yang Y; Wang Y; Wu HL; Li H; He XY
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Jun; 14(6):445-8. PubMed ID: 22738453
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA.
    Dikow N; Nygren AO; Schouten JP; Hartmann C; Krämer N; Janssen B; Zschocke J
    Mol Cell Probes; 2007 Jun; 21(3):208-15. PubMed ID: 17303379
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
    Henkhaus RS; Kim SJ; Kimonis VE; Gold JA; Dykens EM; Driscoll DJ; Butler MG
    Genet Test Mol Biomarkers; 2012 Mar; 16(3):178-86. PubMed ID: 21977908
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome.
    Kim B; Park Y; Cho SI; Kim MJ; Chae JH; Kim JY; Seong MW; Park SS
    Ann Lab Med; 2022 Jan; 42(1):79-88. PubMed ID: 34374352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
    Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
    Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
    Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
    Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT
    Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of Prader-Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13.
    Chang CW; Hsu HK; Kao CC; Huang JY; Kuo PL
    Int J Gynaecol Obstet; 2014 Apr; 125(1):18-21. PubMed ID: 24434231
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA
    Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
    Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
    Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C; Coll MD; Villatoro S; Gabau E; Kamli A; Martínez MJ; Poyatos D; Guitart M
    Eur J Med Genet; 2007; 50(1):11-20. PubMed ID: 17095305
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.
    Bittel DC; Kibiryeva N; Butler MG
    Genet Test; 2007; 11(4):467-75. PubMed ID: 18294067
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effectiveness of multiplex ligation-dependent probe amplification assay used for detecting deletion of Prader-Willi syndrome.
    Shao H; Lip V; Wu BL
    Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):64-7. PubMed ID: 15719045
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prader-Willi and Angelman syndromes: case series diagnosed by MS-MLPA assay].
    Rios-Flores IM; Bobadilla-Morales L; Peña Padilla C; Corona-Rivera A; Acosta-Fernández E; Santana-Hernández J; Brukman-Jiménez SA; Corona Rivera JR
    Rev Med Inst Mex Seguro Soc; 2021 Jun; 59(2):170-178. PubMed ID: 34232598
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays.
    Liu W; Zhang R; Wei J; Zhang H; Yu G; Li Z; Chen M; Sun X
    Cytogenet Genome Res; 2015; 146(1):9-18. PubMed ID: 26184742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.