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PUBMED FOR HANDHELDS

Journal Abstract Search


281 related items for PubMed ID: 694691

  • 1. Chondrodysplasia punctata. Report of parent-to-child transmission.
    Jenkins T, Noll B.
    S Afr Med J; 1978 Jul 01; 54(1):22-5. PubMed ID: 694691
    [Abstract] [Full Text] [Related]

  • 2. Chondrodysplasia punctata. Conradi-Hünermann syndrome.
    Edidin DV, Esterly NB, Bamzai AK, Fretzin DF.
    Arch Dermatol; 1977 Oct 01; 113(10):1431-4. PubMed ID: 911172
    [Abstract] [Full Text] [Related]

  • 3. Conradi-Hunermann syndrome: a case report.
    Louvar RD, Block WM, Martin LR.
    Clin Pediatr (Phila); 1974 Aug 01; 13(8):680-5. PubMed ID: 4448037
    [No Abstract] [Full Text] [Related]

  • 4. [Cataract in chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome)].
    Thiel HJ, Manzke H, Gunschera H.
    Klin Monbl Augenheilkd; 1969 Apr 01; 154(4):536-45. PubMed ID: 5354428
    [No Abstract] [Full Text] [Related]

  • 5. Prenatal sonographic diagnosis of non-rhizomelic chondrodysplasia punctata.
    Sherer DM, Glantz JC, Allen TA, Lonardo F, Metlay LA.
    Obstet Gynecol; 1994 May 01; 83(5 Pt 2):858-60. PubMed ID: 8159377
    [Abstract] [Full Text] [Related]

  • 6. Chondrodysplasia punctata. Report of two cases.
    Andersen PE, Justesen P.
    Skeletal Radiol; 1987 May 01; 16(3):223-6. PubMed ID: 3589739
    [Abstract] [Full Text] [Related]

  • 7. A severely affected female infant with x-linked dominant chondrodysplasia punctata: a case report and a brief review of the literature.
    Rakheja D, Read CP, Hull D, Boriack RL, Timmons CF.
    Pediatr Dev Pathol; 2007 May 01; 10(2):142-8. PubMed ID: 17378690
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of nonrhizomelic chondrodysplasia punctata (Conradi-Hünermann syndrome).
    Pryde PG, Bawle E, Brandt F, Romero R, Treadwell MC, Evans MI.
    Am J Med Genet; 1993 Sep 01; 47(3):426-31. PubMed ID: 8135294
    [Abstract] [Full Text] [Related]

  • 9. Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?
    Mortier GR, Messiaen LM, Espeel M, Smets KJ, Vanzieleghem BD, Roels F, De Paepe AM.
    Pediatr Radiol; 1998 Oct 01; 28(10):790-3. PubMed ID: 9799302
    [Abstract] [Full Text] [Related]

  • 10. Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndrome.
    Lindenthal B, Repgen R, Emons D, Lentze MJ, von Bergmann K, Lütjohann D.
    Klin Padiatr; 2004 Oct 01; 216(2):67-9. PubMed ID: 15106076
    [Abstract] [Full Text] [Related]

  • 11. Ichthyosis and keratotic follicular plugs containing dystrophic calcification in newborns: distinctive histopathologic features of x-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle syndrome).
    Hoang MP, Carder KR, Pandya AG, Bennett MJ.
    Am J Dermatopathol; 2004 Feb 01; 26(1):53-8. PubMed ID: 14726822
    [Abstract] [Full Text] [Related]

  • 12. Guess what! X-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle Syndrome).
    Krisp A, König A, Hoffmann R, Happle R.
    Eur J Dermatol; 2001 Feb 01; 11(4):389-91. PubMed ID: 11458930
    [No Abstract] [Full Text] [Related]

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  • 17. Conradi-Hünermann disease. Case report and mini-review.
    Paltzik RL, Ente G, Penzer PH, Goldblum LM.
    Cutis; 1982 Feb 01; 29(2):174-180. PubMed ID: 7060406
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  • 19. Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case report.
    Benaicha A, Dommergues M, Jouannic JM, Jacquette A, Alexandre M, Le Merrer M, Ducou Le Pointe H, Garel C.
    Ultrasound Obstet Gynecol; 2009 Dec 01; 34(6):724-6. PubMed ID: 19856318
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