000 01372 a2200433 4500
005 20250512082848.0
264 0 _c19850619
008 198506s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.22.2.131
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNorth, C
245 0 0 _aThe clinical features of the Cohen syndrome: further case reports.
_h[electronic resource]
260 _bJournal of medical genetics
_cApr 1985
300 _a131-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aFacial Expression
650 0 4 _aFemale
650 0 4 _aFingers
_xabnormalities
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aMicrocephaly
_xgenetics
650 0 4 _aObesity
_xgenetics
650 0 4 _aPedigree
650 0 4 _aRetinal Degeneration
_xgenetics
650 0 4 _aSyndrome
650 0 4 _aTooth Abnormalities
_xgenetics
700 1 _aPatton, M A
700 1 _aBaraitser, M
700 1 _aWinter, R M
773 0 _tJournal of medical genetics
_gvol. 22
_gno. 2
_gp. 131-4
856 4 0 _uhttps://doi.org/10.1136/jmg.22.2.131
_zAvailable from publisher's website
999 _c3995513
_d3995513