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Publikováno v:
Clinical Genetics. 29:516-522
An isolated case of Duchenne muscular dystrophy in a 15-year-old retarded girl with a de novo t(X;2) (p21.2;q37) translocation is described. Her clinical history is presented, with particular emphasis on CK level determinations made at several differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04bc50fa7ab3fad3f2567d9be7a114b5
https://doi.org/10.1111/j.1399-0004.1986.tb00553.x
https://doi.org/10.1111/j.1399-0004.1986.tb00553.x
