| 000 | 01782 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250513151154.0 | ||
| 264 | 0 | _c19981026 | |
| 008 | 199810s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aYoung, T L | |
| 245 | 0 | 0 |
_aCanadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cAug 1998 |
||
| 300 |
_a461-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBlindness _xcongenital |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 3 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFingers _xabnormalities |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aIntelligence Tests |
| 650 | 0 | 4 |
_aKidney _xabnormalities |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aNewfoundland and Labrador |
| 650 | 0 | 4 |
_aObesity _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPolydactyly _xgenetics |
| 650 | 0 | 4 |
_aRetinitis Pigmentosa _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aToes _xabnormalities |
| 700 | 1 | _aWoods, M O | |
| 700 | 1 | _aParfrey, P S | |
| 700 | 1 | _aGreen, J S | |
| 700 | 1 | _aO'Leary, E | |
| 700 | 1 | _aHefferton, D | |
| 700 | 1 | _aDavidson, W S | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 78 _gno. 5 _gp. 461-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d _zAvailable from publisher's website |
| 999 |
_c9679520 _d9679520 |
||