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kw.\*:("Christ Siemens Touraine syndrome")

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A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasiaTARIQ, Muhammad; WASIF, Naveed; AYUB, Muhammad et al.EJD. European journal of dermatology. 2007, Vol 17, Num 3, pp 209-212, issn 1167-1122, 4 p.Article

X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian familiesVISINONI, Atila F; DE SOUZA, Ricardo L. R; FREIRE-MAIA, Newton et al.American journal of medical genetics. 2003, Vol 122A, Num 1, pp 51-55, issn 0148-7299, 5 p.Article

CARRIER DETECTION IN CHRIST-SIEMENS-TOURAINE SYNDROME (X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA)FREIRE MAIA N; PINHEIRO M.1982; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 4; PP. 672-674; BIBL. 26 REF.Article

Christ-Siemens-Touraine-Syndrom = Christ-Siemens-Touraine syndromeLOTH, M; WAIBEL, M; ALBRECHT, G et al.Hautarzt. 1998, Vol 49, Num 6, pp 505-508, issn 0017-8470Article

Dysplasie ectodermique: proposition de prise en charge prothétique = Ectodermal dysplasia: prosthodontic rehabilitation clinical reportALLOH AMICHIA, Yomin Cécile; BAMBA, Aboudramane; LE GUEHENNEC, Laurent et al.Actualités odonto-stomatologiques. 2010, Num 250, pp 175-186, issn 0001-7817, 12 p.Article

Skin symptoms in four ectodermal dysplasia syndromes including two case reports of Rapp-Hodgkin-SyndromeKNAUDT, Bjorn; VOLZ, Thomas; KRUG, Markus et al.EJD. European journal of dermatology. 2012, Vol 22, Num 5, pp 605-613, issn 1167-1122, 9 p.Article

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