000 01442 a2200409 4500
005 20250517073209.0
264 0 _c20170104
008 201701s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.37553
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRonzoni, Luisa
245 0 0 _aInterstitial 6q25 microdeletion syndrome: ARID1B is the key gene.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMay 2016
300 _a1257-61 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAcyltransferases
_xgenetics
650 0 4 _aChild
650 0 4 _aChromosomes, Human, Pair 6
_xgenetics
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aCorpus Callosum
_xphysiopathology
650 0 4 _aDNA-Binding Proteins
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHearing Loss
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aSpeech-Language Pathology
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aTagliaferri, Francesco
700 1 _aTucci, Arianna
700 1 _aBaccarin, Marco
700 1 _aEsposito, Susanna
700 1 _aMilani, Donatella
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 170A
_gno. 5
_gp. 1257-61
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.37553
_zAvailable from publisher's website
999 _c25619995
_d25619995