| 000 | 01604 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250513035750.0 | ||
| 264 | 0 | _c19951011 | |
| 008 | 199510s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/ajmg.1320570246 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTaschner, P E | |
| 245 | 0 | 0 |
_aCarrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis). _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cJun 1995 |
||
| 300 |
_a333-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 16 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Carrier Screening |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInbreeding |
| 650 | 0 | 4 | _aLinkage Disequilibrium |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNetherlands |
| 650 | 0 | 4 |
_aNeuronal Ceroid-Lipofuscinoses _xdiagnosis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aProbability |
| 650 | 0 | 4 | _aReproducibility of Results |
| 650 | 0 | 4 | _aRisk Factors |
| 700 | 1 | _ade Vos, N | |
| 700 | 1 | _aPost, J G | |
| 700 | 1 | _aMeijers-Heijboer, E J | |
| 700 | 1 | _aHofman, I | |
| 700 | 1 | _aLoonen, M C | |
| 700 | 1 | _aPinckers, A J | |
| 700 | 1 | _aBleeker-Wagemakers, E M | |
| 700 | 1 | _aGardiner, R M | |
| 700 | 1 | _aBreuning, M H | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 57 _gno. 2 _gp. 333-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.1320570246 _zAvailable from publisher's website |
| 999 |
_c7667787 _d7667787 |
||