000 | 01992 a2200565 4500 | ||
---|---|---|---|
005 | 20250516113506.0 | ||
264 | 0 | _c20130327 | |
008 | 201303s 0 0 eng d | ||
022 | _a1096-7206 | ||
024 | 7 |
_a10.1016/j.ymgme.2012.09.008 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aNiida, Yo | |
245 | 0 | 0 |
_aApplying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis. _h[electronic resource] |
260 |
_bMolecular genetics and metabolism _cNov 2012 |
||
300 |
_a580-5 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aArthritis _xdiagnosis |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aBiological Assay |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 |
_aCoffin-Lowry Syndrome _xdiagnosis |
650 | 0 | 4 |
_aCollagen Type II _xgenetics |
650 | 0 | 4 |
_aConnective Tissue Diseases _xdiagnosis |
650 | 0 | 4 |
_aDNA Restriction Enzymes _xmetabolism |
650 | 0 | 4 | _aElectrophoresis, Polyacrylamide Gel |
650 | 0 | 4 |
_aExodeoxyribonucleases _xgenetics |
650 | 0 | 4 | _aExons |
650 | 0 | 4 |
_aHearing Loss, Sensorineural _xdiagnosis |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 |
_aNucleic Acid Heteroduplexes _xanalysis |
650 | 0 | 4 |
_aRecQ Helicases _xgenetics |
650 | 0 | 4 | _aReproducibility of Results |
650 | 0 | 4 |
_aRetinal Detachment _xdiagnosis |
650 | 0 | 4 |
_aRibosomal Protein S6 Kinases, 90-kDa _xgenetics |
650 | 0 | 4 | _aSensitivity and Specificity |
650 | 0 | 4 | _aSilver Staining |
650 | 0 | 4 |
_aWerner Syndrome _xdiagnosis |
650 | 0 | 4 | _aWerner Syndrome Helicase |
700 | 1 | _aKuroda, Mondo | |
700 | 1 | _aMitani, Yusuke | |
700 | 1 | _aOkumura, Akiko | |
700 | 1 | _aYokoi, Ayano | |
773 | 0 |
_tMolecular genetics and metabolism _gvol. 107 _gno. 3 _gp. 580-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ymgme.2012.09.008 _zAvailable from publisher's website |
999 |
_c22144832 _d22144832 |