000 01219 a2200373 4500
005 20250515023438.0
264 0 _c20060523
008 200605s 0 0 eng d
022 _a1424-7860
024 7 _a10.4414/smw.2006.11213
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRamelli, G P
245 0 0 _aBecker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series.
_h[electronic resource]
260 _bSwiss medical weekly
_cMar 2006
300 _a189-93 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild
650 0 4 _aCreatine Kinase
_xanalysis
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMolecular Biology
650 0 4 _aMuscular Dystrophy, Duchenne
_xdiagnosis
650 0 4 _aPathology, Clinical
650 0 4 _aPhenotype
650 0 4 _aSwitzerland
700 1 _aJoncourt, F
700 1 _aLuetschg, J
700 1 _aWeis, J
700 1 _aTolnay, M
700 1 _aBurgunder, J M
773 0 _tSwiss medical weekly
_gvol. 136
_gno. 11-12
_gp. 189-93
856 4 0 _uhttps://doi.org/10.4414/smw.2006.11213
_zAvailable from publisher's website
999 _c16237600
_d16237600