000 01459 a2200421 4500
005 20250515164721.0
264 0 _c20090601
008 200906s 0 0 eng d
022 _a1349-3329
024 7 _a10.1620/tjem.217.307
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPawlowska, Elzbieta
245 0 0 _aMutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth.
_h[electronic resource]
260 _bThe Tohoku journal of experimental medicine
_cApr 2009
300 _a307-12 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAnodontia
_xdiagnostic imaging
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aDNA Primers
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Components
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aHumans
650 0 4 _aMSX1 Transcription Factor
_xgenetics
650 0 4 _aMale
650 0 4 _aMolecular Sequence Data
650 0 4 _aRadiography
650 0 4 _aSequence Analysis, DNA
650 0 4 _aSequence Deletion
700 1 _aJanik-Papis, Katarzyna
700 1 _aWisniewska-Jarosinska, Maria
700 1 _aSzczepanska, Joanna
700 1 _aBlasiak, Janusz
773 0 _tThe Tohoku journal of experimental medicine
_gvol. 217
_gno. 4
_gp. 307-12
856 4 0 _uhttps://doi.org/10.1620/tjem.217.307
_zAvailable from publisher's website
999 _c18781922
_d18781922