BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 26171345)

  • 1. A Case of Autism with Ring Chromosome 14.
    Tajeran M; Baghbani F; Hassanzadeh-Nazarabadi M
    Iran J Public Health; 2013 Nov; 42(11):1316-20. PubMed ID: 26171345
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series.
    Ghasemi MR; Zargari P; Sadeghi H; Bagheri S; Sadeghgi B; Mirfakhraie R; Ekrami M; Mohammadi Sarvaleh S; Hashemi Gorji F; Razjouyan K; Omrani D; Kim HG; Miryounesi M
    Iran J Child Neurol; 2022; 16(2):117-128. PubMed ID: 35497098
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
    Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder.
    Reddy KS
    BMC Med Genet; 2005 Jan; 6():3. PubMed ID: 15655077
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autism with del15p.11.1: case report with a new cytogenetic finding.
    Caglayan AO; Gumus H
    Genet Couns; 2010; 21(2):199-204. PubMed ID: 20681220
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature.
    Charalsawadi C; Maisrikhaw W; Praphanphoj V; Wirojanan J; Hansakunachai T; Roongpraiwan R; Sombuntham T; Ruangdaraganon N; Limprasert P
    Cytogenet Genome Res; 2014; 144(1):1-8. PubMed ID: 25171325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency and the type of chromosomal abnormalities in patients with primary amenorrhea in northeast of iran.
    Mohajertehran F; Ghodsi K; Hafizi L; Rezaee A
    Iran J Basic Med Sci; 2013 Apr; 16(4):643-7. PubMed ID: 24250944
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency and the type of chromosomal abnormalities in patients with primary amenorrhea in northeast of iran.
    Mohajertehran F; Ghodsi K; Hafizi L; Rezaee A
    Iran J Basic Med Sci; 2013 Apr; 16(4):634-9. PubMed ID: 24250941
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.
    Ramanathan S; Woodroffe A; Flodman PL; Mays LZ; Hanouni M; Modahl CB; Steinberg-Epstein R; Bocian ME; Spence MA; Smith M
    BMC Med Genet; 2004 Apr; 5():10. PubMed ID: 15090072
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.
    Ghasemi Firouzabadi S; Vameghi R; Kariminejad R; Darvish H; Banihashemi S; Firouzkouhi Moghaddam M; Jamali P; Farbod Mofidi Tehrani H; Dehghani H; Raeisoon MR; Narooie-Nejad M; Jamshidi J; Tafakhori A; Sadabadi S; Behjati F
    Int J Mol Cell Med; 2016; 5(4):236-245. PubMed ID: 28357200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
    Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7.
    Tsai LP; Lee KF; Fang JS; Liu IY
    Mol Cytogenet; 2011 Feb; 4(1):5. PubMed ID: 21303521
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
    Abu-Amero KK; Hellani AM; Salih MA; Seidahmed MZ; Elmalik TS; Zidan G; Bosley TM
    BMC Med Genet; 2010 Sep; 11():135. PubMed ID: 20858261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.
    Bolton PF; Veltman MW; Weisblatt E; Holmes JR; Thomas NS; Youings SA; Thompson RJ; Roberts SE; Dennis NR; Browne CE; Goodson S; Moore V; Brown J
    Psychiatr Genet; 2004 Sep; 14(3):131-7. PubMed ID: 15318025
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A cytogenetic study of nonpolymalformed patients with mental retardation of clinically undefined etiology: application of a high resolution banding technique.
    Kikkawa K; Narahara K; Kimoto H
    Acta Med Okayama; 1989 Apr; 43(2):105-14. PubMed ID: 2728904
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic risk factors for autism-spectrum disorders: a systematic review based on systematic reviews and meta-analysis.
    Wei H; Zhu Y; Wang T; Zhang X; Zhang K; Zhang Z
    J Neural Transm (Vienna); 2021 Jun; 128(6):717-734. PubMed ID: 34115189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Subtelomeric region of chromosome 2 in patients with autism spectrum disorders.
    Barbosa-Gonçalves A; Vendrame-Goloni CB; Martins AL; Fett-Conte AC
    Genet Mol Res; 2008 Jun; 7(2):527-33. PubMed ID: 18752177
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
    Su PH; Chen CP; Su YN; Chen SJ; Lin LL; Chen JY
    Genet Mol Res; 2013 Apr; 12(2):1311-7. PubMed ID: 23661454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spectral karyotyping study of chromosome abnormalities in human leukemia.
    Zhao L; Hayes K; Khan Z; Glassman A
    Cancer Genet Cytogenet; 2001 Jun; 127(2):143-7. PubMed ID: 11425454
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.