000 01497 a2200469 4500
005 20250517170815.0
264 0 _c20180207
008 201802s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.38404
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHelm, Benjamin M
245 0 0 _aThe role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odyssey.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cOct 2017
300 _a2814-2820 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aGuanine Nucleotide Exchange Factors
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xdiagnosis
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPrognosis
650 0 4 _aSyndrome
650 0 4 _aYoung Adult
700 1 _aPowis, Zoe
700 1 _aPrada, Carlos E
700 1 _aCasasbuenas-Alarcon, Olga L
700 1 _aBalmakund, Tonya
700 1 _aSchaefer, G B
700 1 _aKahler, Stephen G
700 1 _aKaylor, Julie
700 1 _aWinter, Susan
700 1 _aZarate, Yuri A
700 1 _aSchrier Vergano, Samantha A
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 173
_gno. 10
_gp. 2814-2820
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.38404
_zAvailable from publisher's website
999 _c27473227
_d27473227