000 01302 a2200409 4500
005 20250517195945.0
264 0 _c20190111
008 201901s 0 0 eng d
022 _a0973-7693
024 7 _a10.1007/s12098-018-2632-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aYesodharan, Dhanya
245 0 0 _aGoltz-Gorlin Syndrome: Revisiting the Clinical Spectrum.
_h[electronic resource]
260 _bIndian journal of pediatrics
_cDec 2018
300 _a1067-1072 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAcyltransferases
_xgenetics
650 0 4 _aAdult
650 0 4 _aFemale
650 0 4 _aFocal Dermal Hypoplasia
_xdiagnosis
650 0 4 _aGenes, Dominant
650 0 4 _aGenes, X-Linked
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aIndia
650 0 4 _aInfant
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPrenatal Diagnosis
700 1 _aBüschenfelde, Uta Meyer Zum
700 1 _aKutsche, Kerstin
700 1 _aMohandas Nair, K
700 1 _aNampoothiri, Sheela
773 0 _tIndian journal of pediatrics
_gvol. 85
_gno. 12
_gp. 1067-1072
856 4 0 _uhttps://doi.org/10.1007/s12098-018-2632-1
_zAvailable from publisher's website
999 _c28027447
_d28027447