000 01496 a2200493 4500
005 20250513094018.0
264 0 _c19960925
008 199609s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.33.4.300
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNewbury-Ecob, R A
245 0 0 _aHolt-Oram syndrome: a clinical genetic study.
_h[electronic resource]
260 _bJournal of medical genetics
_cApr 1996
300 _a300-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aArm
_xabnormalities
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aElectrocardiography
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Linkage
650 0 4 _aHand Deformities, Congenital
_xgenetics
650 0 4 _aHeart Defects, Congenital
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aRadius
_xabnormalities
650 0 4 _aShoulder
_xabnormalities
650 0 4 _aSyndrome
650 0 4 _aThumb
_xabnormalities
700 1 _aLeanage, R
700 1 _aRaeburn, J A
700 1 _aYoung, I D
773 0 _tJournal of medical genetics
_gvol. 33
_gno. 4
_gp. 300-7
856 4 0 _uhttps://doi.org/10.1136/jmg.33.4.300
_zAvailable from publisher's website
999 _c8727367
_d8727367