These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

266 related items for PubMed ID: 8267001

  • 1. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.
    Happle R, Daniëls O, Koopman RJ.
    Am J Med Genet; 1993 Oct 01; 47(5):710-3. PubMed ID: 8267001
    [Abstract] [Full Text] [Related]

  • 2. Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.
    Lindor NM, Michels VV, Hoppe DA, Driscoll DJ, Leavitt JA, Dewald GW.
    Am J Med Genet; 1992 Sep 01; 44(1):61-5. PubMed ID: 1519653
    [Abstract] [Full Text] [Related]

  • 3. Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?
    Bird LM, Krous HF, Eichenfield LF, Swalwell CI, Jones MC.
    Am J Med Genet; 1994 Nov 01; 53(2):141-8. PubMed ID: 7856638
    [Abstract] [Full Text] [Related]

  • 4. Another observation of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesions.
    Kono T, Migita T, Koyama S, Seki I.
    J Hum Genet; 1999 Nov 01; 44(1):63-8. PubMed ID: 9929982
    [Abstract] [Full Text] [Related]

  • 5. A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations.
    Seven M, Suyugül Z, Yüksel A, Geçkinli B, Hacihanefioğlu S, Cenani A.
    Turk J Pediatr; 1998 Nov 01; 40(4):593-601. PubMed ID: 10028871
    [Abstract] [Full Text] [Related]

  • 6. Microphthalmia with linear skin defects syndrome.
    García-Rabasco A, De-Unamuno B, Martínez F, Febrer-Bosch I, Alegre-de-Miquel V.
    Pediatr Dermatol; 2013 Nov 01; 30(6):e230-1. PubMed ID: 22612277
    [Abstract] [Full Text] [Related]

  • 7. Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.
    Lindsay EA, Grillo A, Ferrero GB, Roth EJ, Magenis E, Grompe M, Hultén M, Gould C, Baldini A, Zoghbi HY.
    Am J Med Genet; 1994 Jan 15; 49(2):229-34. PubMed ID: 8116674
    [Abstract] [Full Text] [Related]

  • 8. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.
    al-Gazali LI, Mueller RF, Caine A, Antoniou A, McCartney A, Fitchett M, Dennis NR.
    J Med Genet; 1990 Jan 15; 27(1):59-63. PubMed ID: 2308157
    [Abstract] [Full Text] [Related]

  • 9. MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome.
    Mücke J, Happle R, Theile H.
    Am J Med Genet; 1995 May 22; 57(1):117-8. PubMed ID: 7645589
    [No Abstract] [Full Text] [Related]

  • 10. Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?
    Naritomi K, Izumikawa Y, Nagataki S, Fukushima Y, Wakui K, Niikawa N, Hirayama K.
    Am J Med Genet; 1992 Jul 15; 43(5):839-43. PubMed ID: 1642272
    [Abstract] [Full Text] [Related]

  • 11. Anterior segment developmental anomalies in a 33-week-old fetus with MIDAS syndrome.
    Herwig MC, Loeffler KU, Gembruch U, Kuchelmeister K, Müller AM.
    Pediatr Dev Pathol; 2014 Jul 15; 17(6):491-5. PubMed ID: 25291437
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. MIDAS (microphthalmia, dermal aplasia, sclerocornea) syndrome with central nervous system abnormalities.
    Carman KB, Yakut A, Sabuncu I, Yarar C.
    Clin Dysmorphol; 2009 Oct 15; 18(4):234-5. PubMed ID: 19726975
    [No Abstract] [Full Text] [Related]

  • 14. Microphthalmia with linear skin defects: a case report and review.
    Sharma VM, Ruiz de Luzuriaga AM, Waggoner D, Greenwald M, Stein SL.
    Pediatr Dermatol; 2008 Oct 15; 25(5):548-52. PubMed ID: 18950397
    [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 Oct 15; 50(6):421-31. PubMed ID: 17845869
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.