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Journal Abstract Search

112 related items for PubMed ID: 3402627

  • 1. A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification.
    Tolmie JL, Browne BH, McGettrick PM, Stephenson JB.
    Eye (Lond); 1988; 2 ( Pt 3)():297-303. PubMed ID: 3402627
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  • 3. Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.
    Crow YJ, McMenamin J, Haenggeli CA, Hadley DM, Tirupathi S, Treacy EP, Zuberi SM, Browne BH, Tolmie JL, Stephenson JB.
    Neuropediatrics; 2004 Feb; 35(1):10-9. PubMed ID: 15002047
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  • 4. [CHILD syndrome in a mother and daughter].
    Happle R, Karlić D, Steijlen PM.
    Hautarzt; 1990 Feb; 41(2):105-8. PubMed ID: 2318640
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  • 5. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance.
    Pinheiro M, Freire-Maia N, Gollop TR.
    Am J Med Genet; 1985 Jan; 20(1):197-202. PubMed ID: 2982262
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  • 6. [Hypotrichosis congenita hereditaria Maria Unna].
    Wirth G, Bindewald I, Küster W, Goerz G.
    Hautarzt; 1985 Oct; 36(10):577-80. PubMed ID: 4066319
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  • 7. CHANDS: the curly hair-ankyloblepharon-nail dysplasia syndrome.
    Baughman FA.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):100-2. PubMed ID: 5173251
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  • 8. Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype.
    Avrahami L, Maas S, Pasmanik-Chor M, Rainshtein L, Magal N, Smitt J, van Marle J, Shohat M, Basel-Vanagaite L.
    Clin Genet; 2008 Jul; 74(1):47-53. PubMed ID: 18445049
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  • 15. [Follicular atrophoderma, hypotrichosis, and multiple milia associated with minimal osteo-cartilaginous dystrophies. Familial study of 3 cases].
    Meynadier J, Guilhou JJ, Barnéon G, Malbos S, Guillot B.
    Ann Dermatol Venereol; 1979 May; 106(5):497-501. PubMed ID: 496212
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  • 16. Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findings.
    Silengo M, Lerone M, Romeo G, Calcagno E, Martucciello G, Jasonni V.
    Am J Med Genet; 1993 Nov 01; 47(6):931-3. PubMed ID: 8279493
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  • 17. [Recessive inherited alopecia and nail dystrophy with heterozygote manifestation].
    Klostermann GF, Jörgensen G.
    Arch Klin Exp Dermatol; 1966 Nov 01; 227(1):505-8. PubMed ID: 5984794
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  • 18. Autosomal dominant hypoparathyroidism with intracranial calcification outside the basal ganglia.
    McLeod DR, Hanley DA, McArthur RG.
    Am J Med Genet; 1989 Jan 01; 32(1):32-5. PubMed ID: 2705481
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  • 19. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B, Hundeiker M.
    Fortschr Med; 1979 Nov 22; 97(44):2018-22. PubMed ID: 511082
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  • 20. Trichoodontoonychial dysplasia--a new meso-ectodermal dysplasia.
    Pinheiro M, Freire-Maia N, Roth AJ.
    Am J Med Genet; 1983 May 22; 15(1):67-70. PubMed ID: 6859125
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