340 related articles for article (PubMed ID: 17890436)
1. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
White HE; Hall VJ; Cross NC
Clin Chem; 2007 Nov; 53(11):1960-2. PubMed ID: 17890436
[TBL] [Abstract][Full Text] [Related]
2. Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome.
White HE; Durston VJ; Harvey JF; Cross NC
Clin Chem; 2006 Jun; 52(6):1005-13. PubMed ID: 16574761
[TBL] [Abstract][Full Text] [Related]
3. A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.
Chotai KA; Payne SJ
J Med Genet; 1998 Jun; 35(6):472-5. PubMed ID: 9643288
[TBL] [Abstract][Full Text] [Related]
4. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
Zeschnigk M; Schmitz B; Dittrich B; Buiting K; Horsthemke B; Doerfler W
Hum Mol Genet; 1997 Mar; 6(3):387-95. PubMed ID: 9147641
[TBL] [Abstract][Full Text] [Related]
5. A rapid and accurate methylation-sensitive high-resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patients.
Ribeiro Ferreira I; Darleans Dos Santos Cunha W; Henrique Ferreira Gomes L; Azevedo Cintra H; Lopes Cabral Guimarães Fonseca L; Ferreira Bastos E; Clinton Llerena J; Farias Meira de Vasconcelos Z; da Cunha Guida L
Mol Genet Genomic Med; 2019 Jun; 7(6):e637. PubMed ID: 31033246
[TBL] [Abstract][Full Text] [Related]
6. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis.
Kubota T; Aradhya S; Macha M; Smith AC; Surh LC; Satish J; Verp MS; Nee HL; Johnson A; Christan SL; Ledbetter DH
J Med Genet; 1996 Dec; 33(12):1011-4. PubMed ID: 9004133
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. High-resolution melting for accurate assessment of DNA methylation.
Dahl C; Guldberg P
Clin Chem; 2007 Nov; 53(11):1877-8. PubMed ID: 17954495
[No Abstract] [Full Text] [Related]
9. Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
Glenn CC; Saitoh S; Jong MT; Filbrandt MM; Surti U; Driscoll DJ; Nicholls RD
Am J Hum Genet; 1996 Feb; 58(2):335-46. PubMed ID: 8571960
[TBL] [Abstract][Full Text] [Related]
10. Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients.
Promkan M; Teingtat S; Stheinkijkarnchai A; Wasant P; Patmasiriwat P
Clin Chem Lab Med; 2007; 45(8):972-80. PubMed ID: 17867985
[TBL] [Abstract][Full Text] [Related]
11. A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.
Zeschnigk M; Lich C; Buiting K; Doerfler W; Horsthemke B
Eur J Hum Genet; 1997; 5(2):94-8. PubMed ID: 9195159
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.
Schweizer J; Zynger D; Francke U
Hum Mol Genet; 1999 Apr; 8(4):555-66. PubMed ID: 10072422
[TBL] [Abstract][Full Text] [Related]
14. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
Ozçelik T; Leff S; Robinson W; Donlon T; Lalande M; Sanjines E; Schinzel A; Francke U
Nat Genet; 1992 Dec; 2(4):265-9. PubMed ID: 1303277
[TBL] [Abstract][Full Text] [Related]
15. [Molecular genetic study of causes of the Prader-Willi and Angelman syndrome].
Capková CP; Vrtĕl R; Santavá A; Zapletalová J; Krsiaková J; Hyjánek J; Santavý J
Cas Lek Cesk; 2005; 144(2):113-8. PubMed ID: 15807298
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
Dittrich B; Robinson WP; Knoblauch H; Buiting K; Schmidt K; Gillessen-Kaesbach G; Horsthemke B
Hum Genet; 1992 Nov; 90(3):313-5. PubMed ID: 1487250
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Allelic dropout can cause false-positive results for Prader-Willi and Angelman syndrome testing.
Hussain Askree S; Hjelm LN; Ali Pervaiz M; Adam M; Bean LJ; Hedge M; Coffee B
J Mol Diagn; 2011 Jan; 13(1):108-12. PubMed ID: 21227401
[TBL] [Abstract][Full Text] [Related]
20. A modified MS-PCR approach to diagnose patients with Prader-Willi and Angelman syndrome.
Dos Santos JF; Mota LR; Rocha PH; Ferreira de Lima RL
Mol Biol Rep; 2016 Nov; 43(11):1221-1225. PubMed ID: 27535666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
