157 related articles for article (PubMed ID: 16896070)
1. Multiple displacement amplification improves PGD for fragile X syndrome.
Burlet P; Frydman N; Gigarel N; Kerbrat V; Tachdjian G; Feyereisen E; Bonnefont JP; Frydman R; Munnich A; Steffann J
Mol Hum Reprod; 2006 Oct; 12(10):647-52. PubMed ID: 16896070
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers.
Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JD
Prenat Diagn; 2001 Jun; 21(6):504-11. PubMed ID: 11438958
[TBL] [Abstract][Full Text] [Related]
4. Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?
Reches A; Malcov M; Ben-Yosef D; Azem F; Amit A; Yaron Y
Prenat Diagn; 2009 Jan; 29(1):57-61. PubMed ID: 19097038
[TBL] [Abstract][Full Text] [Related]
5. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.
Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I
Prenat Diagn; 1999 Dec; 19(13):1223-30. PubMed ID: 10660959
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. 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]
9. 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]
10. Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests.
Kieffer E; Nicod JC; Gardes N; Kastner C; Becker N; Celebi C; Pirrello O; Rongières C; Koscinski I; Gosset P; Moutou C
Eur J Hum Genet; 2016 Feb; 24(2):221-7. PubMed ID: 25966634
[TBL] [Abstract][Full Text] [Related]
11. Closely linked polymorphic marker: successful application in preimplantation genetic diagnosis for beta-thalassemia.
Deng J; Zhuang GL; Peng WL; Zhou CQ; Li J; Fang C; Li SP; Chen Y; Tong DY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):391-5. PubMed ID: 16086275
[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. Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.
Vrettou C; Traeger-Synodinos J; Tzetis M; Palmer G; Sofocleous C; Kanavakis E
Hum Mutat; 2004 May; 23(5):513-21. PubMed ID: 15108284
[TBL] [Abstract][Full Text] [Related]
14. FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.
Rajan-Babu IS; Lian M; Cheah FSH; Chen M; Tan ASC; Prasath EB; Loh SF; Chong SS
Expert Rev Mol Med; 2017 Jul; 19():e10. PubMed ID: 28720156
[TBL] [Abstract][Full Text] [Related]
15. Multiple displacement amplification on single cell and possible PGD applications.
Hellani A; Coskun S; Benkhalifa M; Tbakhi A; Sakati N; Al-Odaib A; Ozand P
Mol Hum Reprod; 2004 Nov; 10(11):847-52. PubMed ID: 15465849
[TBL] [Abstract][Full Text] [Related]
16. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
Ren Z; Zeng HT; Xu YW; Zhuang GL; Deng J; Zhang C; Zhou CQ
Fertil Steril; 2009 Feb; 91(2):359-64. PubMed ID: 18359022
[TBL] [Abstract][Full Text] [Related]
17. Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.
Ren Z; Zhou C; Xu Y; Deng J; Zeng H; Zeng Y
Mol Hum Reprod; 2007 Jun; 13(6):431-6. PubMed ID: 17439955
[TBL] [Abstract][Full Text] [Related]
18. Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.
Kakourou G; Dhanjal S; Mamas T; Serhal P; Delhanty JD; SenGupta SB
Fertil Steril; 2010 Oct; 94(5):1674-9. PubMed ID: 20171614
[TBL] [Abstract][Full Text] [Related]
19. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
Malcov M; Ben-Yosef D; Schwartz T; Mey-Raz N; Azem F; Lessing JB; Amit A; Yaron Y
Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
[TBL] [Abstract][Full Text] [Related]
20. Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.
Charalsawadi C; Sripo T; Limprasert P
J Med Assoc Thai; 2005 Aug; 88(8):1057-61. PubMed ID: 16404832
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]