000 01092 a2200337 4500
005 20250511162748.0
264 0 _c19770425
008 197704s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.13.6.449
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGardner, R J
245 0 0 _aLowe's syndrome: identification of carriers by lens examination.
_h[electronic resource]
260 _bJournal of medical genetics
_cDec 1976
300 _a449-54 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aCataract
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aOculocerebrorenal Syndrome
_xgenetics
650 0 4 _aRenal Tubular Transport, Inborn Errors
_xgenetics
700 1 _aBrown, N
773 0 _tJournal of medical genetics
_gvol. 13
_gno. 6
_gp. 449-54
856 4 0 _uhttps://doi.org/10.1136/jmg.13.6.449
_zAvailable from publisher's website
999 _c1025768
_d1025768