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.
86 related articles for article (PubMed ID: 1003175)
41. [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]
42. Lowe's syndrome: identification of carriers by lens examination. Gardner RJ; Brown N J Med Genet; 1976 Dec; 13(6):449-54. PubMed ID: 1018304 [TBL] [Abstract][Full Text] [Related]
43. Myotonic dystrophy- early detection and genetic counselling by T. Schubert et al. Bundey S J Neurol; 1982; 226(4):295. PubMed ID: 6174712 [No Abstract] [Full Text] [Related]
44. The hazards of pregnancy in myotonic muscular dystrophy. Webb DA Mater Med Pol; 1979; 11(4):394-7. PubMed ID: 553993 [No Abstract] [Full Text] [Related]
46. [Development, problems and results of specialty-specific genetic counseling at the Neurology Clinic of the Karl Marx University]. Bachmann H Psychiatr Neurol Med Psychol (Leipz); 1987 Nov; 39(11):641-50. PubMed ID: 3441572 [TBL] [Abstract][Full Text] [Related]
47. Electroretinography in the evaluation of childhood myotonic dystrophy. Breningstall GN; Smith SA; Purple RL Pediatr Neurol; 1985; 1(4):238-41. PubMed ID: 3880409 [TBL] [Abstract][Full Text] [Related]