000 01340 a2200397 4500
005 20250516112449.0
264 0 _c20130621
008 201306s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.35627
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKariminejad, Ariana
245 0 0 _aAphonia, microstomia, deafness, retinal dystrophy, duplicated halluces and intellectual disability.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cNov 2012
300 _a2756-62 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aAphonia
_xdiagnosis
650 0 4 _aChild, Preschool
650 0 4 _aConsanguinity
650 0 4 _aDeafness
_xdiagnosis
650 0 4 _aFacies
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xdiagnosis
650 0 4 _aMale
650 0 4 _aMicrostomia
_xdiagnosis
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aRetinal Dystrophies
_xdiagnosis
650 0 4 _aSyndrome
700 1 _aHennekam, Raoul C M
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 158A
_gno. 11
_gp. 2756-62
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.35627
_zAvailable from publisher's website
999 _c22116714
_d22116714