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166 related items for PubMed ID: 20981770

  • 1.
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  • 2. Cognitive-behavioral features of children with Wolf-Hirschhorn syndrome: preliminary report of 12 cases.
    Fisch GS, Battaglia A, Parrini B, Youngblom J, Simensen R.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):252-6. PubMed ID: 18932225
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  • 3. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M, Murdolo M, Marangi G, Pecile V, Galasso C, Mazzanti L, Neri G.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):257-69. PubMed ID: 18932124
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  • 4. Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.
    South ST, Hannes F, Fisch GS, Vermeesch JR, Zollino M.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):270-4. PubMed ID: 18932125
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  • 5. Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profile.
    Fisch GS, Carpenter N, Howard-Peebles PN, Holden JJ, Tarleton J, Simensen R, Battaglia A.
    Am J Intellect Dev Disabil; 2012 Mar 15; 117(2):167-79. PubMed ID: 22515830
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  • 6. Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.
    Hannes F, Drozniewska M, Vermeesch JR, Haus O.
    Eur J Med Genet; 2010 Mar 15; 53(3):136-40. PubMed ID: 20197130
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  • 7. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
    Battaglia A, Filippi T, Carey JC.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):246-51. PubMed ID: 18932224
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  • 9. Clinical features in adult patient with Wolf-Hirschhorn syndrome.
    Martínez-Quintana E, Rodríguez-González F.
    Morphologie; 2014 Jun 15; 98(321):86-9. PubMed ID: 24656633
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  • 10. The behavioral phenotype of the idic(15) syndrome.
    Battaglia A, Parrini B, Tancredi R.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):448-55. PubMed ID: 20981774
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  • 11. Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
    South ST, Whitby H, Battaglia A, Carey JC, Brothman AR.
    Eur J Hum Genet; 2008 Jan 15; 16(1):45-52. PubMed ID: 17726485
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  • 12. Mouse models of Wolf-Hirschhorn syndrome.
    Simon R, Bergemann AD.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):275-80. PubMed ID: 18932126
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  • 13. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
    Estabrooks LL, Rao KW, Korf B.
    Am J Med Genet; 1993 Jan 01; 45(1):97-100. PubMed ID: 8418669
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  • 14. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C, Lo-Castro A, Lalli C, Nardone AM, Gullotta F, Curatolo P.
    J Child Neurol; 2008 Jul 01; 23(7):802-6. PubMed ID: 18658079
    [Abstract] [Full Text] [Related]

  • 15. Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
    Zollino M, Orteschi D, Ruiter M, Pfundt R, Steindl K, Cafiero C, Ricciardi S, Contaldo I, Chieffo D, Ranalli D, Acquafondata C, Murdolo M, Marangi G, Asaro A, Battaglia D.
    Epilepsia; 2014 Jun 01; 55(6):849-57. PubMed ID: 24738919
    [Abstract] [Full Text] [Related]

  • 16. Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size.
    Fisch GS, Falk RE, Carey JC, Imitola J, Sederberg M, Caravalho KS, South S.
    Am J Med Genet A; 2016 Sep 01; 170(9):2282-91. PubMed ID: 27282419
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  • 17. FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site.
    Johnson VP, Altherr MR, Blake JM, Keppen LD.
    Am J Med Genet; 1994 Aug 01; 52(1):70-4. PubMed ID: 7977466
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  • 18. Impact of chromosome 4p- syndrome on communication and expressive language skills: a preliminary investigation.
    Marshall AT.
    Lang Speech Hear Serv Sch; 2010 Jul 01; 41(3):265-76. PubMed ID: 20421614
    [Abstract] [Full Text] [Related]

  • 19. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
    Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF.
    Am J Med Genet; 1997 Sep 05; 71(4):453-7. PubMed ID: 9286454
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  • 20. Wolf-Hirschhorn (4P-) syndrome in adults.
    Marcelis C, Schrander-Stumpel C, Engelen J, Schoonbrood-Lenssen A, Willemse A, Beemer F, Sigaudy S, Missirian C, Philip N, Fryns JP.
    Genet Couns; 2001 Sep 05; 12(1):35-48. PubMed ID: 11332977
    [Abstract] [Full Text] [Related]

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