| 000 | 01416 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250514030720.0 | ||
| 264 | 0 | _c20020621 | |
| 008 | 200206s 0 0 eng d | ||
| 022 | _a0340-6717 | ||
| 024 | 7 |
_a10.1007/s00439-002-0690-x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMustapha, Mirna | |
| 245 | 0 | 0 |
_aA novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25. _h[electronic resource] |
| 260 |
_bHuman genetics _cApr 2002 |
||
| 300 |
_a348-50 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 17 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 |
_aHearing Loss, Sensorineural _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aRetinitis Pigmentosa _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aChouery, Eliane | |
| 700 | 1 | _aTorchard-Pagnez, Delphine | |
| 700 | 1 | _aNouaille, Sylvie | |
| 700 | 1 | _aKhrais, Awni | |
| 700 | 1 | _aSayegh, Fouad N | |
| 700 | 1 | _aMégarbané, André | |
| 700 | 1 | _aLoiselet, Jacques | |
| 700 | 1 | _aLathrop, Mark | |
| 700 | 1 | _aPetit, Christine | |
| 700 | 1 | _aWeil, Dominique | |
| 773 | 0 |
_tHuman genetics _gvol. 110 _gno. 4 _gp. 348-50 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-002-0690-x _zAvailable from publisher's website |
| 999 |
_c11844939 _d11844939 |
||