BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 19747340)

  • 1. Monoallelic expression on autosomes may explain an unusual heritable form of pigmentary mosaicism: a historical case revisited.
    Happle R
    Clin Exp Dermatol; 2009 Oct; 34(7):834-7. PubMed ID: 19747340
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pigmentary mosaicism of the hyperpigmented type in two half-brothers.
    Horn D; Happle R; Neitzel H; Kunze J
    Am J Med Genet; 2002 Sep; 112(1):65-9. PubMed ID: 12239723
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Skin manifestations in a case of trisomy 16 mosaicism.
    Ousager LB; Brandrup F; Brasch-Andersen C; Erlendsson A
    Br J Dermatol; 2006 Jan; 154(1):172-6. PubMed ID: 16403114
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two Taiwanese siblings with dyschromatosis universalis hereditaria.
    Wu CY; Huang WH
    Clin Exp Dermatol; 2009 Dec; 34(8):e666-9. PubMed ID: 19538186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Patterns on the skin. New aspects of their embryologic and genetic causes].
    Happle R
    Hautarzt; 2004 Oct; 55(10):960-1, 964-8. PubMed ID: 15351866
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An unusual human mosaic for skin pigmentation.
    Stoll C; Alembik Y; Grosshans E; de Saint Martin A
    Genet Couns; 2002; 13(3):281-7. PubMed ID: 12416635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Piecing together the puzzle of cutaneous mosaicism.
    Paller AS
    J Clin Invest; 2004 Nov; 114(10):1407-9. PubMed ID: 15545989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaicism in human skin. Understanding the patterns and mechanisms.
    Happle R
    Arch Dermatol; 1993 Nov; 129(11):1460-70. PubMed ID: 8239703
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phylloid hypermelanosis: an unusual form of pigmentary mosaicism.
    Happle R
    Dermatology; 2010; 220(2):183-5. PubMed ID: 20110629
    [No Abstract]   [Full Text] [Related]  

  • 10. Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1.
    Miyoshi O; Yabe R; Wakui K; Fukushima Y; Koizumi S; Uchikawa M; Kajii T; Numakura C; Takahashi S; Hayasaka K; Niikawa N
    Am J Med Genet; 2001 Dec; 104(3):250-6. PubMed ID: 11754053
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32.
    Blumen SC; Bevan S; Abu-Mouch S; Negus D; Kahana M; Inzelberg R; Mazarib A; Mahamid A; Carasso RL; Slor H; Withers D; Nisipeanu P; Navon R; Reid E
    Ann Neurol; 2003 Dec; 54(6):796-803. PubMed ID: 14681889
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q.
    Portnoï MF; Boutchneï S; Bouscarat F; Morlier G; Nizard S; Dersarkissian H; Crickx B; Nouchy M; Taillemite JL; Belaich S
    J Med Genet; 1999 Mar; 36(3):246-50. PubMed ID: 10204855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Discoveries and controversies in cutaneous mosaicism.
    Castori M; Tadini G
    G Ital Dermatol Venereol; 2016 Jun; 151(3):251-65. PubMed ID: 27070303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes.
    Taibjee SM; Hall D; Balderson D; Larkins S; Stubbs T; Moss C
    Clin Exp Dermatol; 2009 Oct; 34(7):823-9. PubMed ID: 19438553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
    Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
    Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctata.
    Shirahama S; Miyahara A; Kitoh H; Honda A; Kawase A; Yamada K; Mabuchi A; Kura H; Yokoyama Y; Tsutsumi M; Ikeda T; Tanaka N; Nishimura G; Ohashi H; Ikegawa S
    Hum Genet; 2003 Jan; 112(1):78-83. PubMed ID: 12483303
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Father-to-daughter transmission of focal dermal hypoplasia associated with nonrandom X-inactivation: support for X-linked inheritance and paternal X chromosome mosaicism.
    Gorski JL
    Am J Med Genet; 1991 Sep; 40(3):332-7. PubMed ID: 1951439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypothesis: genes which function in a stochastic lineage commitment process are subject to monoallelic expression.
    Shulman MJ; Wu GE
    Semin Immunol; 1999 Oct; 11(5):369-71. PubMed ID: 10497091
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dohi Memorial Lecture. New aspects of cutaneous mosaicism.
    Happle R
    J Dermatol; 2002 Nov; 29(11):681-92. PubMed ID: 12484429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linear atrophoderma of Moulin: postulation of mosaicism for a predisposing gene.
    Danarti R; Bittar M; Happle R; König A
    J Am Acad Dermatol; 2003 Sep; 49(3):492-8. PubMed ID: 12963915
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.