270 related articles for article (PubMed ID: 15322224)
1. Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease.
Handyside AH; Robinson MD; Simpson RJ; Omar MB; Shaw MA; Grudzinskas JG; Rutherford A
Mol Hum Reprod; 2004 Oct; 10(10):767-72. PubMed ID: 15322224
[TBL] [Abstract][Full Text] [Related]
2. Preimplantation genetic diagnosis of Marfan syndrome using multiple displacement amplification.
Lledó B; Ten J; Galán FM; Bernabeu R
Fertil Steril; 2006 Oct; 86(4):949-55. PubMed ID: 17027361
[TBL] [Abstract][Full Text] [Related]
3. Whole genome amplification from a single cell: a new era for preimplantation genetic diagnosis.
Coskun S; Alsmadi O
Prenat Diagn; 2007 Apr; 27(4):297-302. PubMed ID: 17278176
[TBL] [Abstract][Full Text] [Related]
4. Preimplantation genetic diagnosis of X-linked adrenoleukodystrophy with gender determination using multiple displacement amplification.
Lledó B; Bernabeu R; Ten J; Galán FM; Cioffi L
Fertil Steril; 2007 Nov; 88(5):1327-33. PubMed ID: 17498713
[TBL] [Abstract][Full Text] [Related]
5. Preimplantation genetic diagnosis for beta-thalassemia using single-cell DNA analysis for codons 17 and 26 of beta-globin gene.
Nasri NW; Jamal AR; Abdullah NC; Razi ZR; Mokhtar NM
Arch Med Res; 2009 Jan; 40(1):1-9. PubMed ID: 19064120
[TBL] [Abstract][Full Text] [Related]
6. Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification.
Wells D; Sherlock JK
Prenat Diagn; 1998 Dec; 18(13):1389-401. PubMed ID: 9949439
[TBL] [Abstract][Full Text] [Related]
7. Single cell PCR amplification of microsatellites flanking the COL7A1 gene and suitability for preimplantation genetic diagnosis of Hallopeau-Siemens recessive dystrophic epidermolysis bullosa.
Fassihi H; Renwick PJ; Black C; McGrath JA
J Dermatol Sci; 2006 Jun; 42(3):241-8. PubMed ID: 16500083
[TBL] [Abstract][Full Text] [Related]
8. Preimplantation genetic diagnosis.
Ouhibi N; Olson S; Patton P; Wolf D
Curr Womens Health Rep; 2001 Oct; 1(2):138-42. PubMed ID: 12112960
[TBL] [Abstract][Full Text] [Related]
9. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
Moutou C; Gardes N; Viville S
Eur J Hum Genet; 2002 Apr; 10(4):231-8. PubMed ID: 12032730
[TBL] [Abstract][Full Text] [Related]
10. Singleton birth after preimplantation genetic diagnosis for Huntington disease using whole genome amplification.
Chow JF; Yeung WS; Lau EY; Lam ST; Tong T; Ng EH; Ho PC
Fertil Steril; 2009 Aug; 92(2):828.e7-10. PubMed ID: 19515365
[TBL] [Abstract][Full Text] [Related]
11. Whole-genome multiple displacement amplification from single cells.
Spits C; Le Caignec C; De Rycke M; Van Haute L; Van Steirteghem A; Liebaers I; Sermon K
Nat Protoc; 2006; 1(4):1965-70. PubMed ID: 17487184
[TBL] [Abstract][Full Text] [Related]
12. Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach.
Moutou C; Gardes N; Viville S
Prenat Diagn; 2004 Jul; 24(7):562-9. PubMed ID: 15300750
[TBL] [Abstract][Full Text] [Related]
13. Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
Moutou C; Gardes N; Rongières C; Ohl J; Bettahar-Lebugle K; Wittemer C; Gerlinger P; Viville S
Prenat Diagn; 2001 Jun; 21(6):498-503. PubMed ID: 11438957
[TBL] [Abstract][Full Text] [Related]
14. Biopsy of cleavage stage human embryos and diagnosis of single gene defects by DNA amplification.
Hardy K; Handyside AH
Arch Pathol Lab Med; 1992 Apr; 116(4):388-92. PubMed ID: 1558477
[TBL] [Abstract][Full Text] [Related]
15. Comparison of whole genome amplification methods for further quantitative analysis with microarray-based comparative genomic hybridization.
Lee YS; Tsai CN; Tsai CL; Chang SD; Hsueh DW; Liu CT; Ma CC; Lin SH; Wang TH; Wang HS
Taiwan J Obstet Gynecol; 2008 Mar; 47(1):32-41. PubMed ID: 18400580
[TBL] [Abstract][Full Text] [Related]
16. [Successful preimplantation genetic diagnosis for beta-thalassemia using multiplex nested polymerase chain reaction].
Deng J; Zhuang GL; Peng WL; Zhou CQ; Li J; Liang XY; Deng MF; Zeng YH; Sun HY
Zhonghua Yi Xue Za Zhi; 2005 Mar; 85(12):811-5. PubMed ID: 15949396
[TBL] [Abstract][Full Text] [Related]
17. Multiple displacement amplification for preimplantation genetic diagnosis of fragile X syndrome.
Lee HS; Kim MJ; Lim CK; Cho JW; Song IO; Kang IS
Genet Mol Res; 2011 Nov; 10(4):2851-9. PubMed ID: 22095609
[TBL] [Abstract][Full Text] [Related]
18. Cost-effective one-step PCR amplification of cystic fibrosis delta F508 fragment in a single cell for preimplantation genetic diagnosis.
Tsai YH
Prenat Diagn; 1999 Nov; 19(11):1048-51. PubMed ID: 10589057
[TBL] [Abstract][Full Text] [Related]
19. Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
Harper JC; Wells D; Piyamongkol W; Abou-Sleiman P; Apessos A; Ioulianos A; Davis M; Doshi A; Serhal P; Ranieri M; Rodeck C; Delhanty JD
Prenat Diagn; 2002 Jun; 22(6):525-33. PubMed ID: 12116320
[TBL] [Abstract][Full Text] [Related]
20. Preimplantation genetic diagnosis of inherited disease.
Ao A
Indian J Exp Biol; 1996 Dec; 34(12):1177-82. PubMed ID: 9246906
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
