000 01152 a2200373 4500
005 20250513130212.0
264 0 _c19971120
008 199711s 0 0 eng d
022 _a0041-4301
040 _aNLM
_beng
_cNLM
100 1 _aTaşdemir, H A
245 0 0 _aCorrelation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy.
_h[electronic resource]
260 _bThe Turkish journal of pediatrics
_c
300 _a317-24 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDwarfism
_xgenetics
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aExons
650 0 4 _aHumans
650 0 4 _aMuscular Dystrophies
_xcomplications
650 0 4 _aRegression Analysis
650 0 4 _aSequence Deletion
650 0 4 _aSeverity of Illness Index
700 1 _aTopaloğlu, H
700 1 _aDinçer, P
700 1 _aGöğüş, S
700 1 _aKotiloğlu, E
700 1 _aOzdirim, E
700 1 _aYalaz, K
773 0 _tThe Turkish journal of pediatrics
_gvol. 39
_gno. 3
_gp. 317-24
999 _c9310715
_d9310715