000 01251 a2200373 4500
005 20250516040842.0
264 0 _c20110711
008 201107s 0 0 eng d
022 _a1015-8146
040 _aNLM
_beng
_cNLM
100 1 _aTug, E
245 0 0 _aA Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.
_h[electronic resource]
260 _bGenetic counseling (Geneva, Switzerland)
_c2011
300 _a11-9 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aBrain
_xabnormalities
650 0 4 _aChild
650 0 4 _aChild Behavior Disorders
_xdiagnosis
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 17
_xgenetics
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aFemale
650 0 4 _aGenetic Counseling
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xdiagnosis
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aPhenotype
650 0 4 _aSelf-Injurious Behavior
_xdiagnosis
650 0 4 _aSmith-Magenis Syndrome
_xdiagnosis
700 1 _aCine, N
700 1 _aAydin, H
773 0 _tGenetic counseling (Geneva, Switzerland)
_gvol. 22
_gno. 1
_gp. 11-9
999 _c20875706
_d20875706