000 01481 a2200409 4500
005 20250513094439.0
264 0 _c19961009
008 199610s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/(SICI)1096-8628(19960102)61:1<21::AID-AJMG4>3.0.CO;2-#
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aReish, O
245 0 0 _aDuplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cJan 1996
300 _a21-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aAdult
650 0 4 _aBrain
_xdiagnostic imaging
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aElectroencephalography
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aTomography, X-Ray Computed
700 1 _aBerry, S A
700 1 _aDewald, G
700 1 _aKing, R A
773 0 _tAmerican journal of medical genetics
_gvol. 61
_gno. 1
_gp. 21-5
856 4 0 _uhttps://doi.org/10.1002/(SICI)1096-8628(19960102)61:1<21::AID-AJMG4>3.0.CO;2-#
_zAvailable from publisher's website
999 _c8738969
_d8738969