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 *

134 related articles for article (PubMed ID: 25847229)

  • 1. 4q21 microdeletion in a patient with epilepsy and brain malformations.
    Yano S; McNamara M; Halbach S; Waggoner D
    Am J Med Genet A; 2015 Jun; 167(6):1409-13. PubMed ID: 25847229
    [No Abstract]   [Full Text] [Related]  

  • 2. Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome.
    Tsang E; Rupps R; McGillivray B; Eydoux P; Marra M; Arbour L; Langlois S; Friedman JM; Zahir FR
    Am J Med Genet A; 2012 Oct; 158A(10):2606-9. PubMed ID: 22903878
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
    Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
    J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
    Dobyns WB; Mirzaa G; Christian SL; Petras K; Roseberry J; Clark GD; Curry CJ; McDonald-McGinn D; Medne L; Zackai E; Parsons J; Zand DJ; Hisama FM; Walsh CA; Leventer RJ; Martin CL; Gajecka M; Shaffer LG
    Am J Med Genet A; 2008 Jul; 146A(13):1637-54. PubMed ID: 18536050
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?
    Nucaro A; Pisano T; Chillotti I; Montaldo C; Pruna D
    Clin Genet; 2011 Apr; 79(4):394-5; author reply 396. PubMed ID: 21371014
    [No Abstract]   [Full Text] [Related]  

  • 6. Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions.
    Kasperavičiūtė D; Catarino CB; Chinthapalli K; Clayton LM; Thom M; Martinian L; Cohen H; Adalat S; Bockenhauer D; Pope SA; Lench N; Koltzenburg M; Duncan JS; Hammond P; Hennekam RC; Land JM; Sisodiya SM
    PLoS One; 2011; 6(8):e23182. PubMed ID: 21858020
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Focal Cortical Dysplasia: Relevant for Seizures in Phelan-McDermid Syndrome?
    Jesse S; Huppertz HJ; Ludolph AC; Kassubek J
    Pediatr Neurol; 2021 Feb; 115():7-9. PubMed ID: 33310146
    [No Abstract]   [Full Text] [Related]  

  • 8. Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe.
    Møller RS; Hansen CP; Jackson GD; Ullmann R; Ropers HH; Tommerup N; Tümer Z
    Clin Genet; 2007 Dec; 72(6):593-8. PubMed ID: 17941887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints.
    Kocks A; Endele S; Heller R; Schröder B; Schäfer HJ; Städtler C; Makrigeorgi-Butera M; Winterpacht A
    J Med Genet; 2002 May; 39(5):E23. PubMed ID: 12011164
    [No Abstract]   [Full Text] [Related]  

  • 10. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion.
    Liang JS; Shimojima K; Ohno K; Sugiura C; Une Y; Ohno K; Yamamoto T
    J Med Genet; 2009 Sep; 46(9):645-7. PubMed ID: 19724011
    [No Abstract]   [Full Text] [Related]  

  • 12. De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report.
    Sandal G; Ormeci AR; Oztas S
    Genet Couns; 2013; 24(2):217-22. PubMed ID: 24032293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A 10 Mb duplication in chromosome band 5q31.3-5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis.
    Faguer S; De Sandre-Giovannoli A; Hemery M; Lévy N; Lamant L; Arveiler B; Rooryck C; Prouheze C; Vigouroux A; Chauveau D; Calvas P; Chassaing N
    Eur J Med Genet; 2011; 54(3):310-3. PubMed ID: 21276880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmia.
    Huynh MT; Lambert AS; Tosca L; Petit F; Philippe C; Parisot F; Benoît V; Linglart A; Brisset S; Tran CT; Tachdjian G; Receveur A
    Eur J Med Genet; 2018 Aug; 61(8):459-464. PubMed ID: 29549028
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery.
    Benova B; Jacques TS
    Brain Pathol; 2019 Jul; 29(4):473-484. PubMed ID: 30485578
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Further defining the critical genes for the 4q21 microdeletion disorder.
    Hu X; Chen X; Wu B; Soler IM; Chen S; Shen Y
    Am J Med Genet A; 2017 Jan; 173(1):120-125. PubMed ID: 27604828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations.
    Fejgin K; Nielsen J; Birknow MR; Bastlund JF; Nielsen V; Lauridsen JB; Stefansson H; Steinberg S; Sorensen HB; Mortensen TE; Larsen PH; Klewe IV; Rasmussen SV; Stefansson K; Werge TM; Kallunki P; Christensen KV; Didriksen M
    Biol Psychiatry; 2014 Jul; 76(2):128-37. PubMed ID: 24090792
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems.
    von der Lippe C; Rustad C; Heimdal K; Rødningen OK
    Eur J Med Genet; 2011; 54(3):357-60. PubMed ID: 21187176
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
    Wither RG; Borlot F; MacDonald A; Butcher NJ; Chow EWC; Bassett AS; Andrade DM
    Epilepsia; 2017 Jun; 58(6):1095-1101. PubMed ID: 28448680
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.