000 01089 a2200361 4500
005 20250511222040.0
264 0 _c19910509
008 199105s 0 0 fre d
022 _a0181-5512
040 _aNLM
_beng
_cNLM
100 1 _aAmzallag, T
245 0 0 _a[Progressive cone dystrophy: electrophysiological changes in female carriers].
_h[electronic resource]
260 _bJournal francais d'ophtalmologie
_c1990
300 _a421-8 p.
_bdigital
500 _aPublication Type: Case Reports; English Abstract; Journal Article; Review
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aColor Vision Defects
_xgenetics
650 0 4 _aFemale
650 0 4 _aFollow-Up Studies
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aRetinitis Pigmentosa
_xdiagnosis
650 0 4 _aSex Factors
650 0 4 _aX Chromosome
700 1 _aPuech, B
700 1 _aHache, J C
700 1 _aFrançois, P
773 0 _tJournal francais d'ophtalmologie
_gvol. 13
_gno. 8-9
_gp. 421-8
999 _c2088018
_d2088018