000 01513 a2200469 4500
005 20250515222232.0
264 0 _c20100707
008 201007s 0 0 eng d
022 _a1424-859X
024 7 _a10.1159/000302497
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGijsbers, A C J
245 0 0 _aA subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplication.
_h[electronic resource]
260 _bCytogenetic and genome research
_cJun 2010
300 _a245-9 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 21
650 0 4 _aChromosomes, Human, Pair 3
650 0 4 _aFace
_xabnormalities
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aSegmental Duplications, Genomic
650 0 4 _aSequence Deletion
650 0 4 _aTranslocation, Genetic
650 0 4 _aTrisomy
700 1 _avan Haeringen, A
700 1 _aBosch, C A J
700 1 _aHansson, K
700 1 _aVerschuren, M
700 1 _aBakker, E
700 1 _aBreuning, M H
700 1 _aRuivenkamp, C A L
773 0 _tCytogenetic and genome research
_gvol. 128
_gno. 4
_gp. 245-9
856 4 0 _uhttps://doi.org/10.1159/000302497
_zAvailable from publisher's website
999 _c19787890
_d19787890