000 01527 a2200421 4500
005 20250515061308.0
264 0 _c20070516
008 200705s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.31602
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMencarelli, Maria Antonietta
245 0 0 _aClinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cApr 2007
300 _a858-65 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aCraniofacial Abnormalities
650 0 4 _aFamily Health
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aIntellectual Disability
650 0 4 _aMale
650 0 4 _aMental Disorders
650 0 4 _aNucleic Acid Hybridization
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aSleep Wake Disorders
700 1 _aCaselli, Rossella
700 1 _aPescucci, Chiara
700 1 _aHayek, Giuseppe
700 1 _aZappella, Michele
700 1 _aRenieri, Alessandra
700 1 _aMari, Francesca
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 143A
_gno. 8
_gp. 858-65
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.31602
_zAvailable from publisher's website
999 _c16908534
_d16908534