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Volumn 13, Issue 4, 2003, Pages 343-345

Familial cutis tricolor: A possible example of paradominant inheritance

Author keywords

Cutis tricolor; Didymosis; Paradominant inheritance; Twin spotting

Indexed keywords

ADOLESCENT; ARTICLE; BIRTH DEFECT; BREAST HYPOPLASIA; CASE REPORT; CLINICAL FEATURE; FAMILIAL CUTIS TRICOLOR; FEMALE; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INHERITANCE; MACROPHAGE; MELANOCYTE; PEDIGREE; PHYSICAL EXAMINATION; PIGMENTATION; SKIN DISCOLORATION; TWINS;

EID: 0042160192     PISSN: 11671122     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (21)

References (12)
  • 1
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    • "Cutis tricolor": Congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: An unusual example of twin spotting?
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    • Happle, R.1    Barbi, G.2    Eckert, D.3    Kennerknecht, I.4
  • 2
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    • Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: A further example of twin spotting?
    • De las Heras E, Boixeda JP, Ledo A, Happle R. Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: a further example of twin spotting? Am J Med Genet 1997; 70: 336-7.
    • (1997) Am J Med Genet , vol.70 , pp. 336-337
    • De Las Heras, E.1    Boixeda, J.P.2    Ledo, A.3    Happle, R.4
  • 3
    • 0033818003 scopus 로고    scopus 로고
    • Cutis tricolor: Congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: Further expansion of the phenotype
    • Ruggieri M. Cutis tricolor: congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: further expansion of the phenotype. Eur J Pediatr 2000; 159: 745-9.
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    • Ruggieri, M.1
  • 4
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    • Pigmentary anomalies in ataxia-telangiectasia: A clue to diagnosis and an example of twin spotting
    • Khumalo NP, Joss DV, Huson SM, Burge S. Pigmentary anomalies in ataxia-telangiectasia: a clue to diagnosis and an example of twin spotting. Br J Dermatol 2001; 144: 369-71.
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  • 5
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    • Happle R. Loss of heterozygosity in human skin. J Am Acad Dermatol 1999; 41: 143-61.
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  • 6
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    • Didymosis aplasticosebacea: Coexistence of aplasia cutis congenita and nevus sebaceus may be exploined as a twin spot phenomenon
    • Happle R, König A. Didymosis aplasticosebacea: coexistence of aplasia cutis congenita and nevus sebaceus may be exploined as a twin spot phenomenon. Dermatology 2001; 202: 246-8.
    • (2001) Dermatology , vol.202 , pp. 246-248
    • Happle, R.1    König, A.2
  • 7
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    • Paradominant inheritance: A possible explanation for Becker's pigmented hairy nevus
    • Happle R. Paradominant inheritance: a possible explanation for Becker's pigmented hairy nevus. Eur J Dermatol 1992; 2: 39-40.
    • (1992) Eur J Dermatol , vol.2 , pp. 39-40
    • Happle, R.1
  • 8
    • 0034767511 scopus 로고    scopus 로고
    • Paradominant inheritance may explain familial occurrence of cutis marmorata telangiectatica congenita
    • Danarti R, Happle R, König A. Paradominant inheritance may explain familial occurrence of cutis marmorata telangiectatica congenita. Dermatology 2001; 203: 208-11.
    • (2001) Dermatology , vol.203 , pp. 208-211
    • Danarti, R.1    Happle, R.2    König, A.3
  • 9
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    • Paradominant inheritance, supernumerary nipples and Becker's nevus: Once again!
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  • 10
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    • Familial nevus sebaceus may be explained by paradominant transmission
    • Happle R, König A. Familial nevus sebaceus may be explained by paradominant transmission. Br J Dermatol 1999; 141: 377.
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  • 11
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    • Familial occurrence of nevus sebaceus of Jadassohn: Another case of paradominant inheritance?
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  • 12
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    • Steijlen, P.M.1    Van Steensel, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.