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 |