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3. Some twin spots may not be twins. van Steensel MA. Am J Med Genet A; 2005 Feb 15; 133A(1):113. PubMed ID: 15633168 [No Abstract] [Full Text] [Related]
4. Brief communication: nevus unis lateris and Klippel-Trenaunay-Weber syndrome with the Sturge Weber anomalady in a consanguineous Puerto Rican family. Rivera-Reyes LR, Toro-Solá MA. Bol Asoc Med P R; 1979 Feb 15; 71(2):69-71. PubMed ID: 222308 [No Abstract] [Full Text] [Related]
5. A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance. Ceballos-Quintal JM, Pinto-Escalante D, Castillo-Zapata I. Am J Med Genet; 1996 Jun 14; 63(3):426-7. PubMed ID: 8737646 [Abstract] [Full Text] [Related]
6. [Klippel-Trénaunay-Weber syndrome]. Chessa Ricotti G, Giambi F, Martini R, Pietraperzia M. Pediatr Med Chir; 1984 Jun 14; 6(4):569-71. PubMed ID: 6099889 [Abstract] [Full Text] [Related]
7. [Clinical and genetic characteristics of the Klippel-Trenaunay syndrome]. Kuklík M, Krejcík J, Marík J. Cas Lek Cesk; 1990 Sep 07; 129(36):1133-7. PubMed ID: 2171774 [Abstract] [Full Text] [Related]
8. Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation. Whelan AJ, Watson MS, Porter FD, Steiner RD. Am J Med Genet; 1995 Dec 04; 59(4):492-4. PubMed ID: 8585570 [Abstract] [Full Text] [Related]
9. [Cobb syndrome and Klippel-Trenaunay-Weber syndrome]. Fukutake T, Kawamura M, Moroo I, Asahina M, Hirayama K. Rinsho Shinkeigaku; 1991 Mar 04; 31(3):275-9. PubMed ID: 1654237 [Abstract] [Full Text] [Related]
14. Klippel-Trenaunay syndrome in a monozygotic male twin: supportive evidence for the concept of paradominant inheritance. Hofer T, Frank J, Itin PH. Eur J Dermatol; 2005 Mar 04; 15(5):341-3. PubMed ID: 16172041 [Abstract] [Full Text] [Related]