000 01224 a2200385 4500
005 20250511230225.0
264 0 _c19901106
008 199011s 0 0 eng d
022 _a0009-9163
024 7 _a10.1111/j.1399-0004.1990.tb03561.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGarcía-Dorado, J
245 0 0 _aIncontinentia pigmenti: XXY male with a family history.
_h[electronic resource]
260 _bClinical genetics
_cAug 1990
300 _a128-38 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHumans
650 0 4 _aIncontinentia Pigmenti
_xgenetics
650 0 4 _aInfant
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aSex Chromosome Aberrations
_xgenetics
650 0 4 _aTooth Abnormalities
_xgenetics
650 0 4 _aX Chromosome
700 1 _ade Unamuno, P
700 1 _aFernández-López, E
700 1 _aSalazar Veloz, J
700 1 _aArmijo, M
773 0 _tClinical genetics
_gvol. 38
_gno. 2
_gp. 128-38
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.1990.tb03561.x
_zAvailable from publisher's website
999 _c2214887
_d2214887