000 01470 a2200433 4500
005 20250518010823.0
264 0 _c20200324
008 202003s 0 0 eng d
022 _a1708-8283
024 7 _a10.1177/0883073818811454
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHerriges, John C
245 0 0 _aDelineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature.
_h[electronic resource]
260 _bJournal of child neurology
_c02 2019
300 _a86-93 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Duplication
650 0 4 _aChromosomes, Human, X
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aLanguage Development Disorders
_xgenetics
650 0 4 _aMale
650 0 4 _aMicrocephaly
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
700 1 _aArch, Ellen M
700 1 _aBurgio, Pamela A
700 1 _aBaldwin, Erin E
700 1 _aLaGrave, Danielle
700 1 _aLamb, Allen N
700 1 _aToydemir, Reha M
773 0 _tJournal of child neurology
_gvol. 34
_gno. 2
_gp. 86-93
856 4 0 _uhttps://doi.org/10.1177/0883073818811454
_zAvailable from publisher's website
999 _c29073327
_d29073327