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23. [Congenital form of Steinert's myotonic dystrophy]. Prot J; Badurska B; Wierzbicka I Pediatr Pol; 1969 Jun; 44(6):741-4. PubMed ID: 5802249 [No Abstract] [Full Text] [Related]
24. [Orofacial evaluation with a punctuation scale in patients with myotonic dystrophy (Steinert's disease)]. Noronha CF; Alves Duro LA Arq Neuropsiquiatr; 1995 Sep; 53(3-A):424-31. PubMed ID: 8540816 [TBL] [Abstract][Full Text] [Related]
25. [Muscle response to repeated stimulation in Steinert's disease]. Nappi G; Scamoni C; Moglia A; Arrigo A Riv Neurol; 1973; 43(5):307-14. PubMed ID: 4360652 [No Abstract] [Full Text] [Related]
26. [Clinical study of 8 families with various members affected with myotonic dystrophy of Curschmann Steinert's type]. Morales Asin F; Mostacero Miguel E; García Alvarez F; Olascoaga Urtaza J; Domínguez Arranz M; Morales Asin JM Rev Clin Esp; 1980 Jul; 157(5):313-8. PubMed ID: 7403605 [No Abstract] [Full Text] [Related]
27. [Genetic heterogeneity of myotonic dystrophy]. Kliuchikov VN; Kopshitser IZ Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1641-5. PubMed ID: 6675361 [TBL] [Abstract][Full Text] [Related]
29. A neonatal form of Steinert's myotonic dystrophy in twins after in vitro fertilization. García de Andoin N; Echeverría J; Cobo AM; Rey A; Paisán L; López de Munain A Fertil Steril; 2005 Sep; 84(3):756. PubMed ID: 16169416 [TBL] [Abstract][Full Text] [Related]
30. [Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)]. Marcoz JP J Genet Hum; 1978 Sep; 26(3):237-74. PubMed ID: 739261 [TBL] [Abstract][Full Text] [Related]
31. Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments. Phillips RJ; Hawker SG; Moseley HJ Genet Res; 1973 Aug; 22(1):91-9. PubMed ID: 4588955 [No Abstract] [Full Text] [Related]
32. [Steinert's myotonic dystrophy, a disease with possibility of antenatal diagnosis]. Christodorescu D Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1976; 21(1):65-9. PubMed ID: 1085022 [No Abstract] [Full Text] [Related]
35. [Molecular genetic study in congenital myotonic dystrophy]. Martín P; Sierra J; Losada A; Rufo M; Lucas M Rev Neurol; 1997 Jun; 25(142):833-6. PubMed ID: 9244607 [TBL] [Abstract][Full Text] [Related]
36. [The RFLP of LDR152/PstI in the Chinese and its application to linkage analysis in a myotonic dystrophy family]. Tan J; Qiu XF; Xue JL; Liu ZD; Li YS; Zai CH Yi Chuan Xue Bao; 1991; 18(1):6-11. PubMed ID: 1674205 [TBL] [Abstract][Full Text] [Related]