131 related articles for article (PubMed ID: 11551105)
1. PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensions.
Velinov M; Gu H; Shah K; Genovese M; Duncan C; Kupchik G; Jenkins EC
Genet Test; 2001; 5(2):153-5. PubMed ID: 11551105
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.
Velinov M; Gu H; Genovese M; Duncan C; Brown WT; Jenkins E
Mol Genet Metab; 2000 Jan; 69(1):81-3. PubMed ID: 10655162
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of methylation analysis for diagnostic testing in 258 referrals suspected of Prader-Willi or Angelman syndromes.
Buchholz T; Jackson J; Robson L; Smith A
Hum Genet; 1998 Nov; 103(5):535-9. PubMed ID: 9860294
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. [Quick diagnosis of Prader-Willi and Angelman syndromes by means of methylation test by PCR].
Huerta Rivas C; Barabash Bustelo A; Gallego Merlo J; Ramos Corrales C; Osorio Cabrero A; Robledo Batanero M; Benítez Ortiz J
An Esp Pediatr; 1998 Jun; 48(6):583-6. PubMed ID: 9662840
[TBL] [Abstract][Full Text] [Related]
7. Referral diagnosis of Prader-Willi syndrome and Angelman syndrome based on methylation-specific polymerase chain reaction.
Teng YN; Tsai WH; Wu CJ; Lin SJ; Chen YJ; Kuo PL
J Formos Med Assoc; 2002 Jul; 101(7):488-94. PubMed ID: 12353341
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. [Genetic basis of Prader-Willi and Angelman syndromes: implications for the biologic diagnosis].
Dupont JM; Cuisset L
Arch Pediatr; 1998 Apr; 5(4):418-24. PubMed ID: 9759164
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
Runte M; Färber C; Lich C; Zeschnigk M; Buchholz T; Smith A; Van Maldergem L; Bürger J; Muscatelli F; Gillessen-Kaesbach G; Horsthemke B; Buiting K
Eur J Hum Genet; 2001 Jul; 9(7):519-26. PubMed ID: 11464243
[TBL] [Abstract][Full Text] [Related]
15. Methylation PCR analysis of Prader-Willi syndrome, Angelman syndrome, and control subjects.
Muralidhar B; Butler MG
Am J Med Genet; 1998 Nov; 80(3):263-5. PubMed ID: 9843050
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome].
Iourov IY; Vorsanova SG; Kurinnaaya OS; Kolotii AD; Demidova IA; Kravets VS; Yurov YB
Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(1):49-53. PubMed ID: 24637817
[TBL] [Abstract][Full Text] [Related]
18. FISH analysis in Prader-Willi and Angelman syndrome patients.
Bettio D; Rizzi N; Giardino D; Grugni G; Briscioli V; Selicorni A; Carnevale F; Larizza L
Am J Med Genet; 1995 Mar; 56(2):224-8. PubMed ID: 7625450
[TBL] [Abstract][Full Text] [Related]
19. Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: a cost comparison.
Monaghan KG; Wiktor A; Van Dyke DL
Genet Med; 2002; 4(6):448-50. PubMed ID: 12509717
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
