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Journal Abstract Search

116 related items for PubMed ID: 26518157

  • 1. Congenital hypertrichosis universalis in Mexican female twins.
    Cervantes A, García-Delgado C, Fernández-Ramírez F, Valencia-Herrera A, Kofman S, Morán-Barroso V.
    Int J Dermatol; 2016 Jan; 55(1):e29-31. PubMed ID: 26518157
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  • 2. First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24.
    Hayashi R, Yoshida K, Abe R, Niizeki H, Shimomura Y.
    J Dermatol Sci; 2017 Jan; 85(1):63-65. PubMed ID: 27780627
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  • 11. [Monozygotic heterocaryotic twins: prenatal diagnosis and management].
    Barré M, Le Caignec C, Rival JM, Le Vaillant C, Salomon LJ, Boscher C, Philippe HJ, Ville Y, Vialard F, Winer N.
    Presse Med; 2009 Jan; 38(7-8):1170-3. PubMed ID: 19375887
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  • 12. Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22).
    Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S.
    Clin Genet; 1993 Sep; 44(3):121-8. PubMed ID: 8275569
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  • 18. [Comparative clinical and morphological studies between a newborn with hypertrichosis universalis and infants of similar age with healthy skin. I. A contribution to the etiology of the clinical picture and to the morphology of lanugo].
    Berres HH, Nitschke R.
    Z Kinderheilkd; 1968 May 09; 102(4):327-40. PubMed ID: 5708164
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