000 01468 a2200409 4500
005 20250515000224.0
264 0 _c20060123
008 200601s 0 0 eng d
022 _a1018-4813
024 7 _a10.1038/sj.ejhg.5201487
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKoolen, David A
245 0 0 _aPartial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cNov 2005
300 _a1169-71 p.
_bdigital
500 _aPublication Type: Case Reports; Comment; Letter
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 6
650 0 4 _aFemale
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIris
_xabnormalities
650 0 4 _aPhysical Chromosome Mapping
650 0 4 _aTelomere
700 1 _aKnoers, Nine V A M
700 1 _aNillesen, Willy M
700 1 _aSlabbers, Gordon H P R
700 1 _aSmeets, Dominique
700 1 _ade Leeuw, Nicole
700 1 _aSistermans, Erik A
700 1 _ade Vries, Bert B A
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 13
_gno. 11
_gp. 1169-71
856 4 0 _uhttps://doi.org/10.1038/sj.ejhg.5201487
_zAvailable from publisher's website
999 _c15755488
_d15755488