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4. Variable genetic penetrance of myotonic dystrophy following the diagnosis of idiopathic polyhydramnios. Güler B; Kılıç SH; Kızıltan MY Int J Gynaecol Obstet; 2016 Jul; 134(1):103. PubMed ID: 27039051 [No Abstract] [Full Text] [Related]
5. Congenital Myotonic Dystrophy and Brugada Syndrome: A Report of Two Cases. Gupta K; Kennelly MR; Siddappa AM Am J Case Rep; 2020 Jan; 21():e919867. PubMed ID: 31915326 [TBL] [Abstract][Full Text] [Related]
6. Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2. Kamsteeg EJ; Kress W; Catalli C; Hertz JM; Witsch-Baumgartner M; Buckley MF; van Engelen BG; Schwartz M; Scheffer H Eur J Hum Genet; 2012 Dec; 20(12):1203-8. PubMed ID: 22643181 [TBL] [Abstract][Full Text] [Related]
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9. Myotonic dystrophy type 2: the 2020 update. Meola G Acta Myol; 2020 Dec; 39(4):222-234. PubMed ID: 33458578 [TBL] [Abstract][Full Text] [Related]
10. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring. Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127 [TBL] [Abstract][Full Text] [Related]
11. Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions. Pešović J; Perić S; Brkušanin M; Brajušković G; Rakočević-Stojanović V; Savić-Pavićević D Neurogenetics; 2017 Dec; 18(4):207-218. PubMed ID: 28942489 [TBL] [Abstract][Full Text] [Related]
12. Infection-Induced Rhabdomyolysis in a Pregnant Woman with Undiagnosed Myotonic Dystrophy: A Case Report. Kim HM; Kim H; Cha HH; Kim H; Kim HS; Kim MJ Medicina (Kaunas); 2023 Apr; 59(5):. PubMed ID: 37241056 [TBL] [Abstract][Full Text] [Related]
13. Direct Haplotyping-Based Noninvasive Prenatal Test for Myotonic Dystrophy Type 1 with Large CTG Expansion. Lee JS; Lee KB; Song H; Sun C; Kim MJ; Cho SI; Lee YK; Park SS; Seong MW Clin Chem; 2020 Apr; 66(4):614-615. PubMed ID: 32167563 [No Abstract] [Full Text] [Related]
14. Amniotic fluid secretor typing: validation for use in prenatal prediction of myotonic dystrophy. Teichler-Zallen D; Doherty RA Clin Genet; 1980 Oct; 18(4):257-67. PubMed ID: 6449321 [TBL] [Abstract][Full Text] [Related]
16. Myotonic Dystrophy Type 1 Clinical, Electrophysiological and Molecular Characterization: Experience at Tertiary Care Centre. Khadilkar S; Jagiasi K; Yadav J; Chavan SV; Soni G; Patel B J Assoc Physicians India; 2017 Jun; 65(6):32-37. PubMed ID: 28782311 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review. Geifman-Holtzman O; Fay K Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060 [TBL] [Abstract][Full Text] [Related]
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19. The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1. Ballester-Lopez A; Linares-Pardo I; Koehorst E; Núñez-Manchón J; Pintos-Morell G; Coll-Cantí J; Almendrote M; Lucente G; Arbex A; Magaña JJ; Murillo-Melo NM; Lucia A; Monckton DG; Cumming SA; Ramos-Fransi A; Martínez-Piñeiro A; Nogales-Gadea G Genes (Basel); 2020 Jul; 11(7):. PubMed ID: 32645888 [TBL] [Abstract][Full Text] [Related]
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