000 01720 a2200457 4500
005 20250515005053.0
264 0 _c20060810
008 200608s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.30991
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aJehee, Fernanda Sarquis
245 0 0 _aAn Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cDec 2005
300 _a221-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChromosomes, Human, X
_xgenetics
650 0 4 _aFace
_xabnormalities
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aMicrosatellite Repeats
_xgenetics
650 0 4 _aMicrotubule-Associated Proteins
_xgenetics
650 0 4 _aNucleic Acid Hybridization
_xgenetics
650 0 4 _aPedigree
650 0 4 _aSex Chromosome Aberrations
650 0 4 _aSex Chromosome Disorders
_xgenetics
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aRosenberg, Carla
700 1 _aKrepischi-Santos, Ana Cristina
700 1 _aKok, Fernando
700 1 _aKnijnenburg, Jeroen
700 1 _aFroyen, Guy
700 1 _aVianna-Morgante, Angela M
700 1 _aOpitz, John M
700 1 _aPassos-Bueno, Maria Rita
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 139
_gno. 3
_gp. 221-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.30991
_zAvailable from publisher's website
999 _c15908182
_d15908182