000 01394 a2200433 4500
005 20250514002515.0
264 0 _c20011204
008 200112s 0 0 eng d
022 _a0174-304X
024 7 _a10.1055/s-2001-13877
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMongini, T
245 0 0 _aMyopathy in a patient with chromosome 22q11 deletion.
_h[electronic resource]
260 _bNeuropediatrics
_cApr 2001
300 _a107-9 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aAdolescent
650 0 4 _aBiopsy
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 22
650 0 4 _aCraniofacial Abnormalities
_xdiagnosis
650 0 4 _aCreatine Kinase
_xblood
650 0 4 _aGlycogen
_xmetabolism
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicroscopy, Electron
650 0 4 _aMuscle, Skeletal
_xpathology
650 0 4 _aMuscular Atrophy
_xdiagnosis
650 0 4 _aNeuromuscular Diseases
_xdiagnosis
700 1 _aDoriguzzi, C
700 1 _aArduino, C
700 1 _aBrusco, A
700 1 _aBortolotto, S
700 1 _aMutani, R
700 1 _aPalmucci, L
773 0 _tNeuropediatrics
_gvol. 32
_gno. 2
_gp. 107-9
856 4 0 _uhttps://doi.org/10.1055/s-2001-13877
_zAvailable from publisher's website
999 _c11344558
_d11344558