000 01581 a2200457 4500
005 20250515041842.0
264 0 _c20070329
008 200703s 0 0 eng d
022 _a1018-4813
024 7 _a10.1038/sj.ejhg.5201720
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWillatt, Lionel R
245 0 0 _aNovel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cJan 2007
300 _a45-52 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aCentromere
650 0 4 _aChild
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosomes, Artificial, Bacterial
650 0 4 _aChromosomes, Human, Pair 9
650 0 4 _aCytogenetic Analysis
650 0 4 _aEuchromatin
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Dosage
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aPhenotype
700 1 _aBarber, John C K
700 1 _aClarkson, Amanda
700 1 _aSimonic, Ingrid
700 1 _aRaymond, F Lucy
700 1 _aDocherty, Zoe
700 1 _aOgilvie, Caroline Mackie
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 15
_gno. 1
_gp. 45-52
856 4 0 _uhttps://doi.org/10.1038/sj.ejhg.5201720
_zAvailable from publisher's website
999 _c16564282
_d16564282