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Journal Abstract Search

140 related items for PubMed ID: 4042400

  • 1. A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome.
    Romain DR, Columbano-Green LM, Parfitt RG, Chapman CJ, Smythe RH, Gebbie OB.
    Clin Genet; 1985 Aug; 28(2):166-72. PubMed ID: 4042400
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  • 2. De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome.
    Serville F, Saura R, Billeaud C, Girard S, Choiset A, Longy M, Sandler B.
    Ann Genet; 1987 Aug; 30(3):170-4. PubMed ID: 3499855
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  • 3. Inv dup del(4)(:p14 --> p16.3::p16.3 --> qter) with manifestations of partial duplication 4p and Wolf-Hirschhorn syndrome.
    Kondoh Y, Toma T, Ohashi H, Harada N, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N.
    Am J Med Genet A; 2003 Jul 01; 120A(1):123-6. PubMed ID: 12794704
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  • 4. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M, Borghgraef M, Fryns JP.
    Am J Med Genet; 2001 Dec 01; 104(3):199-203. PubMed ID: 11754044
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  • 6. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Dec 01; 32(1):59-61. PubMed ID: 2751251
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  • 7. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].
    Wilson MG, Towner JW, Coffin GS, Ebbin AJ, Siris E, Brager P.
    Hum Genet; 1981 Dec 01; 59(4):297-307. PubMed ID: 6949855
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  • 8. Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
    Paskulin GA, Riegel M, Cotter PD, Kiss A, Rosa RF, Zen PR, Mombach R, Graziadio C.
    Am J Med Genet A; 2009 Jun 01; 149A(6):1302-7. PubMed ID: 19449429
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  • 10. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
    Finzi S, Pinto CF, Wiggs JL.
    Ophthalmic Genet; 2001 Mar 01; 22(1):35-41. PubMed ID: 11262648
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  • 11. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K, Howard-Peebles PN, Keele D, Friedman JM.
    Am J Med Genet; 1985 Jun 01; 21(2):351-6. PubMed ID: 4014316
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  • 12. Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
    Tassano E, Alpigiani MG, Salvati P, Gimelli S, Lorini R, Gimelli G.
    Gene; 2012 Dec 15; 511(2):338-40. PubMed ID: 23031810
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  • 13. Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.
    Anvret M, Nordenskjöld M, Stolpe L, Johansson L, Bröndum-Nielsen K.
    Hum Genet; 1991 Mar 15; 86(5):481-3. PubMed ID: 2016087
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  • 16. On the deletion 4p16 Wolf-Hirschhorn syndrome.
    Rivas F, Hernandez A, Nazara Z, Fragoso R, Olivares N, Rolon A, Cantu JM.
    Ann Genet; 1979 Mar 15; 22(4):228-31. PubMed ID: 317787
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  • 17. Long-term survival in the Wolf-Hirschhorn (4p-) syndrome.
    Smith SA, Walker AM, Monk AJ, Young ID.
    J Intellect Disabil Res; 1995 Feb 15; 39 ( Pt 1)():83-6. PubMed ID: 7719065
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  • 18. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
    Toncheva D, Genkova P, Tzoneva M, Lozanova T, Angelova E, Mitreva B.
    Acta Paediatr Hung; 1986 Feb 15; 27(1):61-6. PubMed ID: 3730184
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