000 01216 a2200361 4500
005 20250513161313.0
264 0 _c19990413
008 199904s 0 0 eng d
022 _a1381-6810
024 7 _a10.1076/opge.19.4.203.2306
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMeire, F M
245 0 0 _aIsolated Norrie disease in a female caused by a balanced translocation t(X,6).
_h[electronic resource]
260 _bOphthalmic genetics
_cDec 1998
300 _a203-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aBlindness
_xdiagnosis
650 0 4 _aChromosomes, Human, Pair 6
_xgenetics
650 0 4 _aEye
_xdiagnostic imaging
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMicrophthalmos
_xdiagnostic imaging
650 0 4 _aRetinal Detachment
_xdiagnosis
650 0 4 _aTranslocation, Genetic
_xgenetics
650 0 4 _aUltrasonography
650 0 4 _aX Chromosome
_xgenetics
700 1 _aLafaut, B A
700 1 _aSpeleman, F
700 1 _aHanssens, M
773 0 _tOphthalmic genetics
_gvol. 19
_gno. 4
_gp. 203-7
856 4 0 _uhttps://doi.org/10.1076/opge.19.4.203.2306
_zAvailable from publisher's website
999 _c9856989
_d9856989