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Journal Abstract Search

148 related items for PubMed ID: 1334371

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  • 2. Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis.
    Ryan SG, Sherman SL, Terry JC, Sparkes RS, Torres MC, Mackey RW.
    Ann Neurol; 1992 Jun; 31(6):663-8. PubMed ID: 1355335
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  • 5. Molecular genetic reevaluation of the Dutch hyperekplexia family.
    Tijssen MA, Shiang R, van Deutekom J, Boerman RH, Wasmuth JJ, Sandkuijl LA, Frants RR, Padberg GW.
    Arch Neurol; 1995 Jun; 52(6):578-82. PubMed ID: 7763205
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  • 8. A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5q.
    Loftus SK, Edwards SJ, Scherpbier-Heddema T, Buetow KH, Wasmuth JJ, Dixon MJ.
    Hum Mol Genet; 1993 Nov; 2(11):1785-92. PubMed ID: 8281138
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  • 10. [Hyperekplexia -- a treatable neuropediatric disease].
    Freilinger M, Jalowetz S, Reiter E, Schubert MT, Seidl R.
    Klin Padiatr; 2005 Nov; 217(4):220-1. PubMed ID: 16032547
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  • 17. Order of genes on human chromosome 5q with respect to 5q interstitial deletions.
    Huebner K, Nagarajan L, Besa E, Angert E, Lange BJ, Cannizzaro LA, van den Berghe H, Santoli D, Finan J, Croce CM.
    Am J Hum Genet; 1990 Jan; 46(1):26-36. PubMed ID: 2294753
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  • 19. [Stiff baby syndrome is a rare cause of neonatal hypertonicity].
    Rønne MS, Nielsen PB, Mogensen CB.
    Ugeskr Laeger; 2014 Feb 24; 176(9A):V10130627. PubMed ID: 25350416
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