000 01201 a2200373 4500
005 20250516180434.0
264 0 _c20131230
008 201312s 0 0 eng d
022 _a1756-1833
024 7 _a10.1136/bmj.f6610
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKhan, Kamron N
245 0 0 _aPatterns of inheritance, not always easily visible.
_h[electronic resource]
260 _bBMJ (Clinical research ed.)
_cNov 2013
300 _af6610 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild, Preschool
650 0 4 _aCorneal Dystrophies, Hereditary
_xdiagnosis
650 0 4 _aDimethylallyltranstransferase
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aInheritance Patterns
650 0 4 _aMale
650 0 4 _aMutation
_xgenetics
650 0 4 _aPedigree
650 0 4 _aRisk Assessment
650 0 4 _aSequence Analysis, DNA
700 1 _aAli, Manir
700 1 _aPoulter, James A
700 1 _aMcKibbin, Martin
700 1 _aInglehearn, Chris F
773 0 _tBMJ (Clinical research ed.)
_gvol. 347
_gp. f6610
856 4 0 _uhttps://doi.org/10.1136/bmj.f6610
_zAvailable from publisher's website
999 _c23235609
_d23235609