164 related articles for article (PubMed ID: 19687056)
1. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
Altarescu G; Eldar-Geva T; Varshower I; Brooks B; Haran EZ; Margalioth EJ; Levy-Lahad E; Renbaum P
Hum Reprod; 2009 Dec; 24(12):3225-9. PubMed ID: 19687056
[TBL] [Abstract][Full Text] [Related]
2. Polar body-based preimplantation genetic diagnosis for N-acetylglutamate synthase deficiency.
Altarescu G; Brooks B; Eldar-Geva T; Margalioth EJ; Singer A; Levy-Lahad E; Renbaum P
Fetal Diagn Ther; 2008; 24(3):170-6. PubMed ID: 18753752
[TBL] [Abstract][Full Text] [Related]
3. Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1.
Altarescu G; Brooks B; Kaplan Y; Eldar-Geva T; Margalioth EJ; Levy-Lahad E; Renbaum P
Hum Reprod; 2006 Aug; 21(8):2047-51. PubMed ID: 16740526
[TBL] [Abstract][Full Text] [Related]
4. PGD on a recombinant allele: crossover between the TSC2 gene and 'linked' markers impairs accurate diagnosis.
Altarescu G; Eldar Geva T; Brooks B; Margalioth E; Levy-Lahad E; Renbaum P
Prenat Diagn; 2008 Oct; 28(10):929-33. PubMed ID: 18792920
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. First systematic experience of preimplantation genetic diagnosis for de-novo mutations.
Rechitsky S; Pomerantseva E; Pakhalchuk T; Pauling D; Verlinsky O; Kuliev A
Reprod Biomed Online; 2011 Apr; 22(4):350-61. PubMed ID: 21324748
[TBL] [Abstract][Full Text] [Related]
8. Strategies and clinical outcome of 250 cycles of Preimplantation Genetic Diagnosis for single gene disorders.
Fiorentino F; Biricik A; Nuccitelli A; De Palma R; Kahraman S; Iacobelli M; Trengia V; Caserta D; Bonu MA; Borini A; Baldi M
Hum Reprod; 2006 Mar; 21(3):670-84. PubMed ID: 16311287
[TBL] [Abstract][Full Text] [Related]
9. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Preimplantation genetic diagnosis for neurofibromatosis type 1.
Spits C; De Rycke M; Van Ranst N; Joris H; Verpoest W; Lissens W; Devroey P; Van Steirteghem A; Liebaers I; Sermon K
Mol Hum Reprod; 2005 May; 11(5):381-7. PubMed ID: 15833774
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Polar body diagnosis for hemophilia a using multiplex PCR for linked polymorphic markers.
Tomi D; Griesinger G; Schultze-Mosgau A; Eckhold J; Schöpper B; Al-Hasani S; Diedrich K; Schwinger E
J Histochem Cytochem; 2005 Mar; 53(3):277-80. PubMed ID: 15750001
[TBL] [Abstract][Full Text] [Related]
14. [Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].
Wu YL; Wu LQ; Li YP; Liu DE; Zeng Q; Zhu HY; Pan Q; Liang DS; Hu H; Long ZG; Li J; Dai HP; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):246-51. PubMed ID: 17478931
[TBL] [Abstract][Full Text] [Related]
15. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
Zhu HY; Wu LQ; Liang DS; Pan Q; Xia JH
Yi Chuan Xue Bao; 2006 Mar; 33(3):206-12. PubMed ID: 16553208
[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. 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]
18. Preimplantation genetic diagnosis for BRCA1 exon 13 duplication mutation using linked polymorphic markers resulting in a live birth.
Jasper MJ; Liebelt J; Hussey ND
Prenat Diagn; 2008 Apr; 28(4):292-8. PubMed ID: 18302307
[TBL] [Abstract][Full Text] [Related]
19. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.
Percesepe A; Ferrari M; Coviello D; Zanussi M; Castagni M; Neri I; Travi M; Forabosco A; Tedeschi S
Prenat Diagn; 2005 Nov; 25(11):1011-4. PubMed ID: 16231306
[TBL] [Abstract][Full Text] [Related]
20. [Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].
de Die-Smulders CE; Land JA; Dreesen JC; Coonen E; Evers JL; Geraedts JP
Ned Tijdschr Geneeskd; 2004 Dec; 148(50):2491-6. PubMed ID: 15638197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
