000 01337 a2200385 4500
005 20250514211920.0
264 0 _c20050315
008 200503s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.30427
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMathijssen, Inge B
245 0 0 _aIris heterochromia: a variable feature in Verloes-Koulischer-oral-acral syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJan 2005
300 _a338-9 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aAbnormalities, Multiple
_xpathology
650 0 4 _aAlveolar Process
_xabnormalities
650 0 4 _aChild, Preschool
650 0 4 _aHand Deformities, Congenital
_xpathology
650 0 4 _aHumans
650 0 4 _aIris
_xabnormalities
650 0 4 _aLip
_xabnormalities
650 0 4 _aMale
650 0 4 _aMaxilla
_xabnormalities
650 0 4 _aPigmentation Disorders
_xpathology
650 0 4 _aRadiography
650 0 4 _aSyndrome
700 1 _aFryns, Jean-Pierre
700 1 _aDevriendt, Koen
700 1 _aSznajer, Yves
700 1 _aVan Eygen, Maurice
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 132A
_gno. 3
_gp. 338-9
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.30427
_zAvailable from publisher's website
999 _c15263541
_d15263541