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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 10521314)

  • 1. Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.
    Grohmann K; Wienker TF; Saar K; Rudnik-Schöneborn S; Stoltenburg-Didinger G; Rossi R; Novelli G; Nürnberg G; Pfeufer A; Wirth B; Reis A; Zerres K; Hübner C
    Am J Hum Genet; 1999 Nov; 65(5):1459-62. PubMed ID: 10521314
    [No Abstract]   [Full Text] [Related]  

  • 2. Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
    Viollet L; Barois A; Rebeiz JG; Rifai Z; Burlet P; Zarhrate M; Vial E; Dessainte M; Estournet B; Kleinknecht B; Pearn J; Adams RD; Urtizberea JA; Cros DP; Bushby K; Munnich A; Lefebvre S
    Ann Neurol; 2002 May; 51(5):585-92. PubMed ID: 12112104
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
    Viollet L; Zarhrate M; Maystadt I; Estournet-Mathiaut B; Barois A; Desguerre I; Mayer M; Chabrol B; LeHeup B; Cusin V; Billette De Villemeur T; Bonneau D; Saugier-Veber P; Touzery-De Villepin A; Delaubier A; Kaplan J; Jeanpierre M; Feingold J; Munnich A
    Eur J Hum Genet; 2004 Jun; 12(6):483-8. PubMed ID: 15054395
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21.
    Takata RI; Speck Martins CE; Passosbueno MR; Abe KT; Nishimura AL; Da Silva MD; Monteiro A; Lima MI; Kok F; Zatz M
    J Med Genet; 2004 Mar; 41(3):224-9. PubMed ID: 14985388
    [No Abstract]   [Full Text] [Related]  

  • 5. Autosomal dominant distal spinal muscular atrophy: an Italian family not linked to 12q24 and 7p14.
    De Angelis MV; Gatta V; Stuppia L; Passamonti L; Gambi D; Uncini A
    Neuromuscul Disord; 2002 Jan; 12(1):26-30. PubMed ID: 11731281
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p.
    Christodoulou K; Kyriakides T; Hristova AH; Georgiou DM; Kalaydjieva L; Yshpekova B; Ivanova T; Weber JL; Middleton LT
    Hum Mol Genet; 1995 Sep; 4(9):1629-32. PubMed ID: 8541851
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophies.
    Lin X; Zhang QJ; He J; Lin MT; Murong SX; Wang N; Chen WJ
    J Child Neurol; 2014 Aug; 29(8):NP35-9. PubMed ID: 24022109
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.
    Isozumi K; DeLong R; Kaplan J; Deng HX; Iqbal Z; Hung WY; Wilhelmsen KC; Hentati A; Pericak-Vance MA; Siddique T
    Hum Mol Genet; 1996 Sep; 5(9):1377-82. PubMed ID: 8872481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators.
    Melki J; Sheth P; Abdelhak S; Burlet P; Bachelot MF; Lathrop MG; Frezal J; Munnich A
    Lancet; 1990 Aug; 336(8710):271-3. PubMed ID: 1973971
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.
    Grohmann K; Schuelke M; Diers A; Hoffmann K; Lucke B; Adams C; Bertini E; Leonhardt-Horti H; Muntoni F; Ouvrier R; Pfeufer A; Rossi R; Van Maldergem L; Wilmshurst JM; Wienker TF; Sendtner M; Rudnik-Schöneborn S; Zerres K; Hübner C
    Nat Genet; 2001 Sep; 29(1):75-7. PubMed ID: 11528396
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
    Tlili A; Masmoudi S; Dhouib H; Bouaziz S; Rebeh IB; Chouchen J; Turki K; Benzina Z; Charfedine I; Drira M; Ayadi H
    Ann Hum Genet; 2007 Mar; 71(Pt 2):271-5. PubMed ID: 17166180
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage mapping of the spinal muscular atrophy gene.
    Burghes AH; Ingraham SE; Kóte-Jarai Z; Rosenfeld S; Herta N; Nadkarni N; DiDonato CJ; Carpten J; Hurko O; Florence J
    Hum Genet; 1994 Mar; 93(3):305-12. PubMed ID: 8125483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.
    Brzustowicz LM; Lehner T; Castilla LH; Penchaszadeh GK; Wilhelmsen KC; Daniels R; Davies KE; Leppert M; Ziter F; Wood D
    Nature; 1990 Apr; 344(6266):540-1. PubMed ID: 2320125
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K
    J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13.
    Novelli G; Capon F; Tamisari L; Grandi E; Angelini C; Guerrini P; Dallapiccola B
    J Med Genet; 1995 Mar; 32(3):216-9. PubMed ID: 7783173
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
    Gadelha MR; Une KN; Rohde K; Vaisman M; Kineman RD; Frohman LA
    J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
    Kennerson M; Nicholson G; Kowalski B; Krajewski K; El-Khechen D; Feely S; Chu S; Shy M; Garbern J
    Neurology; 2009 Jan; 72(3):246-52. PubMed ID: 19153371
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mapping of the bovine spinal muscular atrophy locus to Chromosome 24.
    Medugorac I; Kemter J; Russ I; Pietrowski D; Nüske S; Reichenbach HD; Schmahl W; Förster M
    Mamm Genome; 2003 Jun; 14(6):383-91. PubMed ID: 12879360
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.
    McEntagart M; Norton N; Williams H; Teare MD; Dunstan M; Baker P; Houlden H; Reilly M; Wood N; Harper PS; Futreal PA; Williams N; Rahman N
    Am J Hum Genet; 2001 May; 68(5):1270-6. PubMed ID: 11294660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in The Netherlands.
    Stalpers XL; Verrips A; Poll-The BT; Cobben JM; Snoeck IN; de Coo IF; Brooks A; Bulk S; Gooskens R; Fock A; Verschuuren-Bemelmans C; Sinke RJ; de Visser M; Lemmink HH
    Neuromuscul Disord; 2013 Jun; 23(6):461-8. PubMed ID: 23566544
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.