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 *

197 related articles for article (PubMed ID: 28777861)

  • 1. [Genotype and phenotype analysis of a child with partial 18q deletion syndrome].
    Shi S; Guo L; Zha Q; Shi Z; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):567-570. PubMed ID: 28777861
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
    Shi S; Pan G; Yang Y; Yan R; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Genotypic and phenotypic analysis of a patient with de novo partial monosomy 18p and partial trisomy 18q].
    Xiao B; Ji X; Ye H; Liu Y; Cao Y; Sun Y; Wei W; Qiu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):484-487. PubMed ID: 31030439
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Accurate detection of a case with Angelman syndrome (type 1) using SNP array].
    Shi S; Lin S; Liao Y; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):824-828. PubMed ID: 27984614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
    Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.
    Nguyen-Minh S; Drossel K; Horn D; Rost I; Spors B; Kaindl AM
    Gene; 2013 Jul; 523(1):92-8. PubMed ID: 23566840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
    Feenstra I; Vissers LE; Orsel M; van Kessel AG; Brunner HG; Veltman JA; van Ravenswaaij-Arts CM
    Am J Med Genet A; 2007 Aug; 143A(16):1858-67. PubMed ID: 17632778
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Phenotypic and genotypic analysis of a fetus carrying an intermediate 22q11.2 deletion encompassing the CRKL gene].
    Lin S; Zheng X; Gu H; Li M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):393-397. PubMed ID: 28604963
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
    Gunn SR; Mohammed M; Reveles XT; Viskochil DH; Palumbos JC; Johnson-Pais TL; Hale DE; Lancaster JL; Hardies LJ; Boespflug-Tanguy O; Cody JD; Leach RJ
    Am J Med Genet A; 2003 Jul; 120A(1):127-35. PubMed ID: 12794705
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Single-nucleotide polymorphism array-based characterization of ring chromosome 18.
    Spreiz A; Guilherme RS; Castellan C; Green A; Rittinger O; Wellek B; Utermann B; Erdel M; Fauth C; Haberlandt E; Kim CA; Kulikowski LD; Meloni VA; Utermann G; Zschocke J; Melaragno MI; Kotzot D
    J Pediatr; 2013 Oct; 163(4):1174-8.e3. PubMed ID: 23876976
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.
    Yapijakis C; Angelopoulou A; Manolakos E; Voumvourakis C
    Adv Exp Med Biol; 2020; 1195():163-166. PubMed ID: 32468472
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiac anomalies in individuals with the 18q deletion syndrome; report of a child with Ebstein anomaly and review of the literature.
    van Trier DC; Feenstra I; Bot P; de Leeuw N; Draaisma JM
    Eur J Med Genet; 2013 Aug; 56(8):426-31. PubMed ID: 23707655
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Chromosome microarray analysis of patients with 18q deletion syndrome].
    Feng J; Hao J; Chen Y; Li F; Han J; Li R; Zhang Y; Lei T; Chen F; Guo Q; Liao C; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):203-7. PubMed ID: 27060316
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations.
    Dostal A; Linnankivi T; Somer M; Kähkönen M; Litzman J; Tienari P
    Int J Immunogenet; 2007 Jun; 34(3):143-7. PubMed ID: 17504501
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
    Bonaglia MC; Fichera M; Marelli S; Romaniello R; Zuffardi O
    Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array].
    Jin Y; Liu X; Li S; Zhou C; Liu X; Song Q; Wang L; Miao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):501-4. PubMed ID: 27455007
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical and genetic analysis of a child with chromosomal 13q32.1-q33.3 deletion].
    Wang H; Huang C; Li L; Liu Y; Wang T; Zhang Y; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1213-1218. PubMed ID: 31813151
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of 2.3-Mb gene locus for congenital aural atresia in 18q22.3 deletion: a case report analyzed by comparative genomic hybridization.
    Dostal A; Nemeckova J; Gaillyova R; Vranova V; Zezulkova D; Lejska M; Slapak I; Dostalova Z; Kuglik P
    Otol Neurotol; 2006 Apr; 27(3):427-32. PubMed ID: 16639285
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.