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 |