| 000 | 01667 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250514224650.0 | ||
| 264 | 0 | _c20050812 | |
| 008 | 200508s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2005.00438.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aJehee, F S | |
| 245 | 0 | 0 |
_aMolecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. _h[electronic resource] |
| 260 |
_bClinical genetics _cJun 2005 |
||
| 300 |
_a503-10 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 11 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 9 |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aCraniosynostoses _xdiagnosis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 700 | 1 | _aJohnson, D | |
| 700 | 1 | _aAlonso, L G | |
| 700 | 1 | _aCavalcanti, D P | |
| 700 | 1 | _ade Sá Moreira, E | |
| 700 | 1 | _aAlberto, F L | |
| 700 | 1 | _aKok, F | |
| 700 | 1 | _aKim, C | |
| 700 | 1 | _aWall, S A | |
| 700 | 1 | _aJabs, E W | |
| 700 | 1 | _aBoyadjiev, S A | |
| 700 | 1 | _aWilkie, A O M | |
| 700 | 1 | _aPassos-Bueno, M R | |
| 773 | 0 |
_tClinical genetics _gvol. 67 _gno. 6 _gp. 503-10 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2005.00438.x _zAvailable from publisher's website |
| 999 |
_c15524274 _d15524274 |
||