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| 005 | 20250515203124.0 | ||
| 264 | 0 | _c20100503 | |
| 008 | 201005s 0 0 eng d | ||
| 022 | _a1469-1809 | ||
| 024 | 7 |
_a10.1111/j.1469-1809.2009.00559.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aReish, Orit | |
| 245 | 0 | 0 |
_aFounder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families. _h[electronic resource] |
| 260 |
_bAnnals of human genetics _cMar 2010 |
||
| 300 |
_a117-25 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aArabs _xgenetics |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKartagener Syndrome _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 700 | 1 | _aSlatkin, Montgomery | |
| 700 | 1 | _aChapman-Shimshoni, Daphne | |
| 700 | 1 | _aElizur, Arnon | |
| 700 | 1 | _aChioza, Barry | |
| 700 | 1 | _aCastleman, Victoria | |
| 700 | 1 | _aMitchison, Hannah M | |
| 773 | 0 |
_tAnnals of human genetics _gvol. 74 _gno. 2 _gp. 117-25 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1469-1809.2009.00559.x _zAvailable from publisher's website |
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_c19448996 _d19448996 |
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