000 01430 a2200421 4500
005 20250516162515.0
264 0 _c20140325
008 201403s 0 0 eng d
022 _a1878-0849
024 7 _a10.1016/j.ejmg.2013.07.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHickey, Scott E
245 0 0 _aMultigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
_h[electronic resource]
260 _bEuropean journal of medical genetics
_cSep 2013
300 _a521-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 4
_xgenetics
650 0 4 _aDevelopmental Disabilities
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aGrowth Disorders
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aSyndrome
700 1 _aBiswas, Sawona
700 1 _aThrush, Devon Lamb
700 1 _aPyatt, Robert E
700 1 _aGastier-Foster, Julie M
700 1 _aAstbury, Caroline
700 1 _aAtkin, Joan
773 0 _tEuropean journal of medical genetics
_gvol. 56
_gno. 9
_gp. 521-5
856 4 0 _uhttps://doi.org/10.1016/j.ejmg.2013.07.004
_zAvailable from publisher's website
999 _c22956793
_d22956793