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 *

180 related articles for article (PubMed ID: 21703560)

  • 1. Interstitial deletions of the short arm of chromosome 4 in a patient with mental retardation and focal seizure.
    Su PH; Lee IC; Chen JY; Chen SJ; Yu JS; Tsao TF
    Pediatr Neonatol; 2011 Jun; 52(3):165-8. PubMed ID: 21703560
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
    Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
    Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mild phenotype in interstitial 4p deletion: another patient and review of the literature.
    Van de Graaf G; Sijstermans JM; Engelen JJ; Schrander-Stumpel CT
    Genet Couns; 1997; 8(1):13-8. PubMed ID: 9101273
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
    Schinzel A; Binkert F; Lillington DM; Sands M; Stocks RJ; Lindenbaum RH; Matthews H; Sheridan H
    J Med Genet; 1991 May; 28(5):352-5. PubMed ID: 1865477
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a mentally retarded boy with a piebald trait, due to maternal insertion, ins(8;4).
    Fujimoto A; Reddy KS; Spinks R
    Am J Med Genet; 1998 Jan; 75(1):78-81. PubMed ID: 9450862
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
    Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial interstitial deletion of chromosome 4 (p15.2p16.1).
    Tonk VS; Jalal SM; Gonzalez J; Kennedy A; Velagaleti GV
    Ann Genet; 2003; 46(4):453-8. PubMed ID: 14659781
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
    Caliebe A; Waltz S; Jenderny J
    Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement.
    Tzschach A; Menzel C; Erdogan F; Istifli ES; Rieger M; Ovens-Raeder A; Macke A; Ropers HH; Ullmann R; Kalscheuer V
    Am J Med Genet A; 2010 Apr; 152A(4):1008-12. PubMed ID: 20358617
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 55(6):849-57. PubMed ID: 24738919
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Array CGH defined interstitial deletion on chromosome 14: a new case.
    Piccione M; Antona V; Scavone V; Malacarne M; Pierluigi M; Grasso M; Corsello G
    Eur J Pediatr; 2010 Jul; 169(7):845-51. PubMed ID: 20087602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation.
    Spranger S; Rommel B; Jauch A; Bodammer R; Mehl B; Bullerdiek J
    Am J Med Genet; 2000 Jul; 93(2):107-9. PubMed ID: 10869111
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial Pitt-Rogers-Danks: two new cases].
    Cabrera López JC; Marti Herrero M; Fernández Burriel M; Toledo L; de Andrés-Cofiño R; Orera MA
    Rev Neurol; 2001 Sep 1-15; 33(5):439-43. PubMed ID: 11727212
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata.
    Bisgaard AM; Rasmussen LN; Møller HU; Kirchhoff M; Bryndorf T
    Clin Dysmorphol; 2007 Apr; 16(2):109-112. PubMed ID: 17351355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation.
    Mikelsaar RV; Varb K; Süvari A; Schinzel A
    J Med Genet; 2001 Jan; 38(1):E2. PubMed ID: 11134241
    [No Abstract]   [Full Text] [Related]  

  • 16. 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; 71(4):453-7. PubMed ID: 9286454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pain insensitivity in a child with a de novo interstitial deletion of the long arm of the chromosome 4: Case report.
    Cascella M; Muzio MR
    Rev Chil Pediatr; 2017 Jun; 88(3):411-416. PubMed ID: 28737203
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
    Caliebe A; Kroes HY; van der Smagt JJ; Martin-Subero JI; Tönnies H; van 't Slot R; Nievelstein RA; Muhle H; Stephani U; Alfke K; Stefanova I; Hellenbroich Y; Gillessen-Kaesbach G; Hochstenbach R; Siebert R; Poot M
    Eur J Med Genet; 2010; 53(4):179-85. PubMed ID: 20382278
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A single gene deletion on 4q28.3: PCDH18--a new candidate gene for intellectual disability?
    Kasnauskiene J; Ciuladaite Z; Preiksaitiene E; Matulevičienė A; Alexandrou A; Koumbaris G; Sismani C; Pepalytė I; Patsalis PC; Kučinskas V
    Eur J Med Genet; 2012 Apr; 55(4):274-7. PubMed ID: 22450339
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.