000 01539 a2200409 4500
005 20250515232438.0
264 0 _c20101115
008 201011s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.33517
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGimelli, Stefania
245 0 0 _aArray-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cAug 2010
300 _a2130-3 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChromosomes, Human, Pair 11
_xgenetics
650 0 4 _aChromosomes, Human, Pair 2
_xgenetics
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aFathers
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aTranslocation, Genetic
_xgenetics
650 0 4 _aWAGR Syndrome
_xgenetics
700 1 _aDivizia, Maria Teresa
700 1 _aLerone, Margherita
700 1 _aBricco, Lara
700 1 _aBéna, Frédérique
700 1 _aAntonarakis, Stylianos E
700 1 _aRavazzolo, Roberto
700 1 _aGimelli, Giorgio
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 152A
_gno. 8
_gp. 2130-3
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.33517
_zAvailable from publisher's website
999 _c19977949
_d19977949