These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 10398260)

  • 1. Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes.
    Steijlen PM; van Steensel MA
    Am J Med Genet; 1999 Aug; 85(4):359-60. PubMed ID: 10398260
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paradominant inheritance may explain familial occurrence of Cutis marmorata telangiectatica congenita.
    Danarti R; Happle R; König A
    Dermatology; 2001; 203(3):208-11. PubMed ID: 11701972
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Large congenital melanocytic nevi may reflect paradominant inheritance implying allelic loss.
    Danarti R; König A; Happle R
    Eur J Dermatol; 2003; 13(5):430-2. PubMed ID: 14693484
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Klippel-Trenaunay syndrome: is it a paradominant trait?
    Happle R
    Br J Dermatol; 1993 Apr; 128(4):465-6. PubMed ID: 8388238
    [No Abstract]   [Full Text] [Related]  

  • 5. 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; 15(5):341-3. PubMed ID: 16172041
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic aspects in Klippel-Trenaunay syndrome].
    Aelvoet GE; Jorens PG; Roelen LM
    Phlebologie; 1991; 44(4):809-14. PubMed ID: 1666678
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Supernumerary nipples occurring together with Becker's naevus: an association involving one common paradominant trait?
    Urbani CE; Betti R
    Hum Genet; 1997 Sep; 100(3-4):388-90. PubMed ID: 9272160
    [No Abstract]   [Full Text] [Related]  

  • 8. Some twin spots may not be twins.
    van Steensel MA
    Am J Med Genet A; 2005 Feb; 133A(1):113. PubMed ID: 15633168
    [No Abstract]   [Full Text] [Related]  

  • 9. 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; 71(2):69-71. PubMed ID: 222308
    [No Abstract]   [Full Text] [Related]  

  • 10. Klippel-Trenaunay syndrome: diagnostic criteria and hypothesis on etiology.
    Oduber CE; van der Horst CM; Hennekam RC
    Ann Plast Surg; 2008 Feb; 60(2):217-23. PubMed ID: 18216519
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increased parental age and number of pregnancies in Klippel-Trenaunay-Weber syndrome.
    Lorda-Sanchez I; Prieto L; Rodriguez-Pinilla E; Martinez-Frias ML
    Ann Hum Genet; 1998 May; 62(Pt 3):235-9. PubMed ID: 9803268
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Association on Sturge Weber and Klippel Trenaunay Weber syndromes. Apropos of 2 cases].
    Guízar Vázquez J; Navarrete Cadena C; Barrón Uribe C; Velázquez E; Armendares S
    Bol Med Hosp Infant Mex; 1979; 36(3):415-24. PubMed ID: 218598
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phakomatosis pigmentovascularis: Clinical findings in 15 patients and review of the literature.
    Fernández-Guarino M; Boixeda P; de Las Heras E; Aboin S; García-Millán C; Olasolo PJ
    J Am Acad Dermatol; 2008 Jan; 58(1):88-93. PubMed ID: 18045734
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Vascular disorders.
    Paller AS
    Dermatol Clin; 1987 Jan; 5(1):239-50. PubMed ID: 3030594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 63(3):426-7. PubMed ID: 8737646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital vascular lesions of the gastrointestinal tract: blue rubber bleb nevus and Klippel-Trenaunay syndromes.
    Arguedas MR; Shore G; Wilcox CM
    South Med J; 2001 Apr; 94(4):405-10. PubMed ID: 11332907
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic aspects of the Klippel-Trenaunay syndrome.
    Aelvoet GE; Jorens PG; Roelen LM
    Br J Dermatol; 1992 Jun; 126(6):603-7. PubMed ID: 1319193
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pathology, symptomatology, localization, age and sex distribution in naevus vasculosus osteohypertrophicus (Klippel-Trenaunay-Parkes-Weber syndrome].
    PETSCHELT E
    Arch Dermatol Syph; 1953; 196(2):155-69. PubMed ID: 13125393
    [No Abstract]   [Full Text] [Related]  

  • 19. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin.
    Happle R
    J Am Acad Dermatol; 1987 Apr; 16(4):899-906. PubMed ID: 3033033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Klippel-Trenaunay and Sturge-Weber syndrome with extensive Mongolian spots, hypoplastic larynx and subglottic stenosis.
    Leung AK; Lowry RB; Mitchell I; Martin S; Cooper DM
    Clin Exp Dermatol; 1988 Mar; 13(2):128-32. PubMed ID: 2850877
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.