000 | 01994 a2200613 4500 | ||
---|---|---|---|
005 | 20250515131103.0 | ||
264 | 0 | _c20081017 | |
008 | 200810s 0 0 eng d | ||
022 | _a1708-8283 | ||
024 | 7 |
_a10.1177/0883073808317730 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aAmador, Claudia | |
245 | 0 | 0 |
_aExpanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. _h[electronic resource] |
260 |
_bJournal of child neurology _cAug 2008 |
||
300 |
_a901-5 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAged |
650 | 0 | 4 |
_aBrain _xpathology |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 |
_aConnexin 43 _xgenetics |
650 | 0 | 4 |
_aCraniofacial Abnormalities _xdiagnosis |
650 | 0 | 4 |
_aExons _xgenetics |
650 | 0 | 4 |
_aEye Abnormalities _xdiagnosis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGait Disorders, Neurologic _xdiagnosis |
650 | 0 | 4 |
_aGenes, Dominant _xgenetics |
650 | 0 | 4 | _aGenetic Counseling |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMagnetic Resonance Imaging |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aNeurologic Examination |
650 | 0 | 4 |
_aParaplegia _xdiagnosis |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPenetrance |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aPrognosis |
650 | 0 | 4 |
_aQuadriplegia _xdiagnosis |
650 | 0 | 4 |
_aSpinal Cord _xpathology |
650 | 0 | 4 |
_aSyndactyly _xdiagnosis |
650 | 0 | 4 |
_aTooth Abnormalities _xdiagnosis |
700 | 1 | _aMathews, Anne M | |
700 | 1 | _aDel Carmen Montoya, Maria | |
700 | 1 | _aLaughridge, Mary E | |
700 | 1 | _aEverman, David B | |
700 | 1 | _aHolden, Kenton R | |
773 | 0 |
_tJournal of child neurology _gvol. 23 _gno. 8 _gp. 901-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1177/0883073808317730 _zAvailable from publisher's website |
999 |
_c18137515 _d18137515 |