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Journal Abstract Search

132 related items for PubMed ID: 2318640

  • 1. [CHILD syndrome in a mother and daughter].
    Happle R, Karlić D, Steijlen PM.
    Hautarzt; 1990 Feb; 41(2):105-8. PubMed ID: 2318640
    [Abstract] [Full Text] [Related]

  • 2. CHILD syndrome in 3 generations: the importance of mild or minimal skin lesions.
    Bittar M, Happle R, Grzeschik KH, Leveleki L, Hertl M, Bornholdt D, König A.
    Arch Dermatol; 2006 Mar; 142(3):348-51. PubMed ID: 16549711
    [Abstract] [Full Text] [Related]

  • 3. [Congenital hypotrichosis and milia with spontaneous regression during adolescence or Oley syndrome: a variant of Bazex-Dupré-Christol syndrome].
    Andreani V, Richard M, Folchetti G, Varennes S, Philip N, Grob JJ.
    Ann Dermatol Venereol; 2000 Mar; 127(3):285-8. PubMed ID: 10804303
    [Abstract] [Full Text] [Related]

  • 4. [Brachyonychia of different types in a mother and daughter].
    Zaun H, Payeur M, Stenger D.
    Hautarzt; 1987 Feb; 38(2):104-6. PubMed ID: 3570776
    [Abstract] [Full Text] [Related]

  • 5. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N, Jordaan FH, Taljaard JJ, Hough SF.
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
    [Abstract] [Full Text] [Related]

  • 6. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndrome.
    Stern JK, Lubinsky MS, Durrie DS, Luckasen JR.
    Am J Med Genet; 1984 May; 18(1):67-77. PubMed ID: 6234802
    [Abstract] [Full Text] [Related]

  • 7. [X-linked dominant chondrodysplasia punctata: an osteocutaneous syndrome].
    Happle R, Kästner H.
    Hautarzt; 1979 Nov; 30(11):590-4. PubMed ID: 521286
    [Abstract] [Full Text] [Related]

  • 8. 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 Nov; 50(6):421-31. PubMed ID: 17845869
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. [CHILD syndrome. Case report of a rare genetic dermatosis].
    Peter C, Meinecke P.
    Hautarzt; 1993 Sep 22; 44(9):590-3. PubMed ID: 8407327
    [Abstract] [Full Text] [Related]

  • 11. [18 q deletion in mother and daughter (author's transl)].
    Sulzer M, Zierler H.
    Wien Klin Wochenschr; 1976 Sep 17; 88(17):571-5. PubMed ID: 997544
    [Abstract] [Full Text] [Related]

  • 12. 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 Sep 17; 2 ( Pt 3)():297-303. PubMed ID: 3402627
    [Abstract] [Full Text] [Related]

  • 13. [The tricho-rhino-phalangeal syndrome (author's transl)].
    Lemke T, Pirsig W.
    Laryngol Rhinol Otol (Stuttg); 1978 Dec 17; 57(12):1112-5. PubMed ID: 732492
    [Abstract] [Full Text] [Related]

  • 14. [Congenital homolateral epidermal hyperplasia and hypoplastic hemidysplasia (splitting of the Solomon's syndrome) (author's transl)].
    Laplanche G, Grosshans E, Gabriel-Robez O, Happle R, Enjolras O.
    Ann Dermatol Venereol; 1980 Dec 17; 107(8-9):729-39. PubMed ID: 7447253
    [Abstract] [Full Text] [Related]

  • 15. Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait.
    Schöpf E, Schulz HJ, Passarge E.
    Birth Defects Orig Artic Ser; 1971 Jun 17; 7(8):219-21. PubMed ID: 4281327
    [Abstract] [Full Text] [Related]

  • 16. Aarskog syndrome: full male and female expression associated with an X-autosome translocation.
    Bawle E, Tyrkus M, Lipman S, Bozimowski D.
    Am J Med Genet; 1984 Mar 17; 17(3):595-602. PubMed ID: 6711610
    [Abstract] [Full Text] [Related]

  • 17. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May 17; 36(1):89-93. PubMed ID: 2333912
    [Abstract] [Full Text] [Related]

  • 18. Congenital hypotrichosis and milia: report of a large family suggesting X-linked dominant inheritance.
    Rapelanoro R, Taïeb A, Lacombe D.
    Am J Med Genet; 1994 Oct 01; 52(4):487-90. PubMed ID: 7747764
    [Abstract] [Full Text] [Related]

  • 19. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome.
    Zabawski EJ, Cohen JB.
    Dermatol Online J; 1999 May 01; 5(1):3. PubMed ID: 10673446
    [Abstract] [Full Text] [Related]

  • 20. [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
    Mende B, Kreysel HW.
    Hautarzt; 1987 Sep 01; 38(9):532-5. PubMed ID: 3692855
    [Abstract] [Full Text] [Related]

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