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Journal Abstract Search

209 related items for PubMed ID: 1404293

  • 1. The acrocallosal syndrome and Greig syndrome are not allelic disorders.
    Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM.
    J Med Genet; 1992 Sep; 29(9):635-7. PubMed ID: 1404293
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  • 2. Acrocallosal syndrome: a new case.
    Lungarotti MS, Marinelli D, Mezzetti D, Caputo N, Calabro A.
    Am J Med Genet; 1991 Jul 01; 40(1):94-6. PubMed ID: 1887856
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  • 3. Four patients including two sisters with the acrocallosal syndrome (agenesis of the corpus callosum in combination with preaxial hexadactyly).
    Schinzel A.
    Hum Genet; 1982 Jul 01; 62(4):382. PubMed ID: 7166318
    [No Abstract] [Full Text] [Related]

  • 4. Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.
    Johnston JJ, Olivos-Glander I, Turner J, Aleck K, Bird LM, Mehta L, Schimke RN, Heilstedt H, Spence JE, Blancato J, Biesecker LG.
    Am J Med Genet A; 2003 Dec 15; 123A(3):236-42. PubMed ID: 14608643
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  • 5. The acrocallosal syndrome in sisters.
    Schinzel A, Kaufmann U.
    Clin Genet; 1986 Nov 15; 30(5):399-405. PubMed ID: 3802558
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  • 6. The acrocallosal syndrome.
    Philip N, Apicella N, Lassman I, Ayme S, Mattei JF, Giraud F.
    Eur J Pediatr; 1988 Feb 15; 147(2):206-8. PubMed ID: 3366141
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  • 7. Spectrum of the acrocallosal syndrome.
    Koenig R, Bach A, Woelki U, Grzeschik KH, Fuchs S.
    Am J Med Genet; 2002 Feb 15; 108(1):7-11. PubMed ID: 11857542
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  • 8. De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models.
    Elson E, Perveen R, Donnai D, Wall S, Black GC.
    J Med Genet; 2002 Nov 15; 39(11):804-6. PubMed ID: 12414818
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  • 10. Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
    van Maldergem L, Wetzburger C, Verloes A, Fourneau C, Gillerot Y.
    Clin Genet; 1992 Jan 15; 41(1):22-4. PubMed ID: 1633641
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  • 12. Further delineation of the acrocallosal syndrome.
    Gelman-Kohan Z, Antonelli J, Ankori-Cohen H, Adar H, Chemke J.
    Eur J Pediatr; 1991 Sep 15; 150(11):797-9. PubMed ID: 1659985
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  • 13. The acrocallosal syndrome in a Turkish boy.
    Yüksel M, Caliskan M, Oğur G, Ozmen M, Dolunay G, Apak S.
    J Med Genet; 1990 Jan 15; 27(1):48-9. PubMed ID: 2308155
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  • 14. Agenesis of the corpus callosum associated with MASA syndrome.
    Boyd E, Schwartz CE, Schroer RJ, May MM, Shapiro SD, Arena JF, Lubs HA, Stevenson RE.
    Clin Dysmorphol; 1993 Oct 15; 2(4):332-41. PubMed ID: 8305964
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  • 17. Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.
    Williams PG, Hersh JH, Yen FF, Barch MJ, Kleinert HE, Kunz J, Kalff-Suske M.
    Clin Genet; 1997 Dec 15; 52(6):436-41. PubMed ID: 9520255
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