000 01198 a2200361 4500
005 20250513030642.0
264 0 _c19940224
008 199402s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320470805
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKennerknecht, I
245 0 0 _aDup(1q)(q42-->qter) syndrome: case report and review of literature.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cDec 1993
300 _a1157-60 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChromosomes, Human, Pair 1
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aFace
_xabnormalities
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aMouth Abnormalities
_xgenetics
650 0 4 _aMultigene Family
650 0 4 _aSyndrome
650 0 4 _aTrisomy
700 1 _aBarbi, G
700 1 _aRodens, K
773 0 _tAmerican journal of medical genetics
_gvol. 47
_gno. 8
_gp. 1157-60
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320470805
_zAvailable from publisher's website
999 _c7506763
_d7506763