These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
152 related articles for article (PubMed ID: 9949443)
1. Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos. Sermon K; Goossens V; Seneca S; Lissens W; De Vos A; Vandervorst M; Van Steirteghem A; Liebaers I Prenat Diagn; 1998 Dec; 18(13):1427-36. PubMed ID: 9949443 [TBL] [Abstract][Full Text] [Related]
2. The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008). van Rij MC; de Koning Gans PA; van Belzen MJ; Roos RA; Geraedts JP; De Rademaeker M; Bijlsma EK; de Die-Smulders CE Clin Genet; 2014 Jan; 85(1):87-95. PubMed ID: 23350580 [TBL] [Abstract][Full Text] [Related]
3. New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications. Moutou C; Gardes N; Viville S Eur J Hum Genet; 2004 Dec; 12(12):1007-14. PubMed ID: 15470361 [TBL] [Abstract][Full Text] [Related]
4. Huntington's Disease: Relationship Between Phenotype and Genotype. Sun YM; Zhang YB; Wu ZY Mol Neurobiol; 2017 Jan; 54(1):342-348. PubMed ID: 26742514 [TBL] [Abstract][Full Text] [Related]
5. Preimplantation genetic diagnosis for Huntington's disease with exclusion testing. Sermon K; De Rijcke M; Lissens W; De Vos A; Platteau P; Bonduelle M; Devroey P; Van Steirteghem A; Liebaers I Eur J Hum Genet; 2002 Oct; 10(10):591-8. PubMed ID: 12357329 [TBL] [Abstract][Full Text] [Related]
6. First preimplantation genetic testing case for monogenic disease in Latvia. Perminov D; Voložonoka L; Korņejeva L; Jokste-Pțmane E; Blumberga A; Krasucka S; Seimuškina N; Kovaļova I; Fodina V Gynecol Endocrinol; 2017; 33(sup1):47-49. PubMed ID: 29264979 [TBL] [Abstract][Full Text] [Related]
7. Low utilization of prenatal and pre-implantation genetic diagnosis in Huntington disease - risk discounting in preventive genetics. Schulman JD; Stern HJ Clin Genet; 2015 Sep; 88(3):220-3. PubMed ID: 25307798 [TBL] [Abstract][Full Text] [Related]
8. Singleton births after routine preimplantation genetic diagnosis using exclusion testing (D4S43 and D4S126) for Huntington's disease. Jasper MJ; Hu DG; Liebelt J; Sherrin D; Watson R; Tremellen KP; Hussey ND Fertil Steril; 2006 Mar; 85(3):597-602. PubMed ID: 16500325 [TBL] [Abstract][Full Text] [Related]
10. Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the delta F508 deletion causing cystic fibrosis in clinical practice. Ray PF; Ao A; Taylor DM; Winston RM; Handyside AH Prenat Diagn; 1998 Dec; 18(13):1402-12. PubMed ID: 9949440 [TBL] [Abstract][Full Text] [Related]
11. Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres. Van Rij MC; De Rademaeker M; Moutou C; Dreesen JC; De Rycke M; Liebaers I; Geraedts JP; De Die-Smulders CE; Viville S; Eur J Hum Genet; 2012 Apr; 20(4):368-75. PubMed ID: 22071896 [TBL] [Abstract][Full Text] [Related]
12. Clinical and counselling implications of preimplantation genetic diagnosis for Huntington's disease in the UK. Lashwood A; Flinter F Hum Fertil (Camb); 2001; 4(4):235-8. PubMed ID: 11719718 [TBL] [Abstract][Full Text] [Related]
13. A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion. Margolis RL; O'Hearn E; Rosenblatt A; Willour V; Holmes SE; Franz ML; Callahan C; Hwang HS; Troncoso JC; Ross CA Ann Neurol; 2001 Sep; 50(3):373-80. PubMed ID: 11558794 [TBL] [Abstract][Full Text] [Related]
14. Risk Assessment for Huntington's Disease for (Future) Offspring Requires Offering Preconceptional CAG Analysis to Both Partners. Tibben A; Dondorp WJ; de Wert GM; de Die-Smulders CE; Losekoot M; Bijlsma EK J Huntingtons Dis; 2019; 8(1):71-78. PubMed ID: 30689590 [TBL] [Abstract][Full Text] [Related]
15. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms. Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771 [TBL] [Abstract][Full Text] [Related]
16. Expansion of a (CAG)n repeat region in a sporadic case of HD. Bozza A; Malagù S; Calzolari E; Novelletto A; Pavoni M; del Senno L Acta Neurol Scand; 1995 Aug; 92(2):132-4. PubMed ID: 7484060 [TBL] [Abstract][Full Text] [Related]
17. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome. Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S77-85. PubMed ID: 11576738 [TBL] [Abstract][Full Text] [Related]
18. [Huntington's chorea: clinical aspects, genetics and current diagnosis]. Spiegel R Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653 [TBL] [Abstract][Full Text] [Related]
19. Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational study. Paulsen JS; Long JD; Ross CA; Harrington DL; Erwin CJ; Williams JK; Westervelt HJ; Johnson HJ; Aylward EH; Zhang Y; Bockholt HJ; Barker RA; Lancet Neurol; 2014 Dec; 13(12):1193-201. PubMed ID: 25453459 [TBL] [Abstract][Full Text] [Related]
20. Reduced allele dropout in single-cell analysis for preimplantation genetic diagnosis of cystic fibrosis. Ray PF; Winston RM; Handyside AH J Assist Reprod Genet; 1996 Feb; 13(2):104-6. PubMed ID: 8688580 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]