000 01420 a2200445 4500
005 20250515210007.0
264 0 _c20110322
008 201103s 0 0 eng d
022 _a1365-2133
024 7 _a10.1111/j.1365-2133.2010.09703.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVan Geel, M
245 0 0 _aPhenotypic variability associated with WNT10A nonsense mutations.
_h[electronic resource]
260 _bThe British journal of dermatology
_cJun 2010
300 _a1403-6 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aEctodermal Dysplasia
_xgenetics
650 0 4 _aFemale
650 0 4 _aHair Diseases
_xgenetics
650 0 4 _aHair Follicle
_xabnormalities
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation, Missense
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aSequence Analysis, DNA
650 0 4 _aWnt Proteins
_xgenetics
650 0 4 _aYoung Adult
700 1 _aGattas, M
700 1 _aKesler, Y
700 1 _aTong, P
700 1 _aYan, H
700 1 _aTran, K
700 1 _aSteijlen, P M
700 1 _aMurrell, D F
700 1 _aVan Steensel, M A M
773 0 _tThe British journal of dermatology
_gvol. 162
_gno. 6
_gp. 1403-6
856 4 0 _uhttps://doi.org/10.1111/j.1365-2133.2010.09703.x
_zAvailable from publisher's website
999 _c19533055
_d19533055