000 01218 a2200361 4500
005 20250513075547.0
264 0 _c19931025
008 199310s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.30.7.604
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPrasher, V P
245 0 0 _aDeletion of chromosome 2 (p11-p13): case report and review.
_h[electronic resource]
260 _bJournal of medical genetics
_cJul 1993
300 _a604-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdult
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aFacial Bones
_xabnormalities
650 0 4 _aGrowth Disorders
_xgenetics
650 0 4 _aHand Deformities, Congenital
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
700 1 _aKrishnan, V H
700 1 _aClarke, D J
700 1 _aMaliszewska, C T
700 1 _aCorbett, J A
773 0 _tJournal of medical genetics
_gvol. 30
_gno. 7
_gp. 604-6
856 4 0 _uhttps://doi.org/10.1136/jmg.30.7.604
_zAvailable from publisher's website
999 _c8410310
_d8410310