000 01530 a2200421 4500
005 20250516111557.0
264 0 _c20130204
008 201302s 0 0 eng d
022 _a1424-859X
024 7 _a10.1159/000342165
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKowalczyk, M
245 0 0 _aAnother rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
_h[electronic resource]
260 _bCytogenetic and genome research
_c2013
300 _a9-16 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormal Karyotype
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Duplication
650 0 4 _aChromosomes, Human, Pair 9
_xgenetics
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aDevelopmental Disabilities
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
700 1 _aTomaszewska, A
700 1 _aPodbioł-Palenta, A
700 1 _aConstantinou, M
700 1 _aWawrzkiewicz-Witkowska, A
700 1 _aKowalski, J
700 1 _aKałużewski, B
700 1 _aZajączek, S
700 1 _aSrebniak, M I
773 0 _tCytogenetic and genome research
_gvol. 139
_gno. 1
_gp. 9-16
856 4 0 _uhttps://doi.org/10.1159/000342165
_zAvailable from publisher's website
999 _c22092793
_d22092793