000 01350 a2200421 4500
005 20250515111024.0
264 0 _c20080402
008 200804s 0 0 eng d
022 _a1015-8146
040 _aNLM
_beng
_cNLM
100 1 _aKoç, A
245 0 0 _aA boy with small supernumerary marker chromosome X identified by FISH.
_h[electronic resource]
260 _bGenetic counseling (Geneva, Switzerland)
_c2007
300 _a393-9 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosomes, Human, X
_xgenetics
650 0 4 _aFingers
_xabnormalities
650 0 4 _aGenetic Markers
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aIntellectual Disability
_xcomplications
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aRNA, Long Noncoding
650 0 4 _aRNA, Untranslated
_xgenetics
650 0 4 _aRing Chromosomes
650 0 4 _aSella Turcica
_xabnormalities
650 0 4 _aSpeech Disorders
_xcomplications
700 1 _aYirmibeş Karaoğuz, M
700 1 _aPala, E
700 1 _aKan, D
700 1 _aKaraer, K
700 1 _aGücüyener, K
700 1 _aPerçin, E F
773 0 _tGenetic counseling (Geneva, Switzerland)
_gvol. 18
_gno. 4
_gp. 393-9
999 _c17791144
_d17791144