| 000 | 01770 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250513065559.0 | ||
| 264 | 0 | _c19931207 | |
| 008 | 199312s 0 0 eng d | ||
| 022 | _a0890-8508 | ||
| 024 | 7 |
_a10.1006/mcpr.1993.1045 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMansfield, E S | |
| 245 | 0 | 0 |
_aFluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status. _h[electronic resource] |
| 260 |
_bMolecular and cellular probes _cAug 1993 |
||
| 300 |
_a311-24 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aDNA Primers |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypoxanthine Phosphoribosyltransferase _xgenetics |
| 650 | 0 | 4 |
_aIntrons _xgenetics |
| 650 | 0 | 4 |
_aLesch-Nyhan Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMultigene Family |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 |
_aPolymerase Chain Reaction _xmethods |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 |
_aRepetitive Sequences, Nucleic Acid _xgenetics |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aBlasband, A | |
| 700 | 1 | _aKronick, M N | |
| 700 | 1 | _aWrabetz, L | |
| 700 | 1 | _aKaplan, P | |
| 700 | 1 | _aRappaport, E | |
| 700 | 1 | _aSartore, M | |
| 700 | 1 | _aParrella, T | |
| 700 | 1 | _aSurrey, S | |
| 700 | 1 | _aFortina, P | |
| 773 | 0 |
_tMolecular and cellular probes _gvol. 7 _gno. 4 _gp. 311-24 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1006/mcpr.1993.1045 _zAvailable from publisher's website |
| 999 |
_c8231633 _d8231633 |
||