BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 24495766)

  • 1. [One case of 2q37 deletion syndrome: clinical and genetic diagnosis].
    Geng Q; Xie JS; Wu WQ; Luo FW; Chen WB
    Zhonghua Er Ke Za Zhi; 2013 Dec; 51(12):934-7. PubMed ID: 24495766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Application of array-CGH and MLPA for detection of 4 cryptic unbalanced translocations].
    Geng Q; Wu W; Luo F; Xu Z; Chen W; Li F; Xie J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):288-92. PubMed ID: 23744316
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Genetic analysis of a case with 2q37 microdeletion syndrome].
    Lian X; Zhang X; Huang M; Lin J; Zeng J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):81-84. PubMed ID: 34964974
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3.
    Mehraein Y; Pfob M; Steinlein O; Aichinger E; Eggert M; Bubendorff V; Mannhart A; Müller S
    Cytogenet Genome Res; 2015; 146(1):33-8. PubMed ID: 26112830
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genotype and phenotype study of two patients with 22q11.2 deletion syndrome].
    Zhu H; Wang A; Zhang H; Ji C; Zhan X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):623-7. PubMed ID: 25297596
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.
    Piccione M; Piro E; Serraino F; Cavani S; Ciccone R; Malacarne M; Pierluigi M; Vitaloni M; Zuffardi O; Corsello G
    Eur J Med Genet; 2012 Apr; 55(4):238-44. PubMed ID: 22406401
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).
    Shim SH; Shim JS; Min K; Lee HS; Park JE; Park SH; Hwang E; Kim M
    Gene; 2014 Jan; 534(1):100-6. PubMed ID: 24095776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.
    Kim MK; Seok HH; Kim YS; Chin MU; Sung SR; Lee WS; Shim SH; Yoon TK
    Gene; 2014 Jan; 534(1):54-9. PubMed ID: 24148559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report.
    Ismail A; Ahid F; Thong MK; Zakaria Z
    J Med Case Rep; 2023 Jun; 17(1):250. PubMed ID: 37296475
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two cases of deletion 2q37 associated with segregation of an unbalanced translocation 2;21: choanal atresia leading to misdiagnosis of CHARGE syndrome.
    Fernández-Rebollo E; Pérez O; Martinez-Bouzas C; Cotarelo-Pérez MC; Garin I; Ruibal JL; Pérez-Nanclares G; Castaño L; de Nanclares GP
    Eur J Endocrinol; 2009 Apr; 160(4):711-7. PubMed ID: 19332529
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features.
    Chen CP; Lin SP; Chern SR; Tsai FJ; Wu PC; Lee CC; Chen LF; Lee MS; Wang W
    Genet Couns; 2010; 21(2):263-7. PubMed ID: 20681230
    [No Abstract]   [Full Text] [Related]  

  • 14. [Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].
    Wu D; Wang H; Zhang H; Hou Q; Qin L; Wang T; Xiao H; Liao S; Wang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):823-6. PubMed ID: 26663057
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.
    Wang T; Mao J; Liu MJ; Choy KW; Li HB; Cram DS; Li H; Chen Y
    Clin Chim Acta; 2014 Mar; 430():129-33. PubMed ID: 24412318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
    Kitsiou-Tzeli S; Sismani C; Ioannides M; Bashiardes S; Ketoni A; Touliatou V; Kolialexi A; Mavrou A; Kanavakis E; Patsalis PC
    Eur J Med Genet; 2007; 50(1):73-8. PubMed ID: 17194633
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome.
    Sakai Y; Souzaki R; Yamamoto H; Matsushita Y; Nagata H; Ishizaki Y; Torisu H; Oda Y; Taguchi T; Shaw CA; Hara T
    BMC Med Genomics; 2014 Apr; 7():19. PubMed ID: 24755370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
    Chen CP; Lin CJ; Chang TY; Chern SR; Wu PS; Chen YT; Su JW; Lee CC; Chen LF; Wang W
    Gene; 2013 Apr; 519(1):164-8. PubMed ID: 23403238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization.
    Yang WX; Pan H; Li L; Wu HR; Wang ST; Bao XH; Jiang YW; Qi Y
    Chin Med J (Engl); 2016 Mar; 129(6):672-8. PubMed ID: 26960370
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.