BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

71 related articles for article (PubMed ID: 27060314)

  • 1. [Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication].
    Zhao J; Gao J; Zhao X; Li L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):617-621. PubMed ID: 38684312
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic analysis of a fetus with Pitt-Hopkins syndrome due to a 18q21.2q21.31 microdeletion].
    Zhang Y; Zeng L; Lin L; Dong X; Lin K; Chen H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):622-625. PubMed ID: 38684313
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genotype and phenotype of chromosome 18p deletion syndrome: Case series.
    Jin Q; Qiang R; Cai B; Wang X; Cai N; Zhen S; Zhai W
    Medicine (Baltimore); 2021 May; 100(18):e25777. PubMed ID: 33950970
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal detection of chromosome 7q deletion with duplication: A case report and literature review.
    Zhu J; Hu J
    Medicine (Baltimore); 2024 Jun; 103(23):e38461. PubMed ID: 38847723
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic analysis of a Chinese pedigree affected with overgrowth syndrome due to a small supernumerary marker chromosome].
    Jin Y; Li S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1425-1429. PubMed ID: 37906154
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of Xp22.31q27.1 Region Variation Detection based on SNP Array Technology.
    Xu L; Wang K; Liu B
    Clin Lab; 2024 Jan; 70(1):. PubMed ID: 38213212
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Prenatal genetic diagnosis of a case with ring chromosome 13].
    Sun L; Wen J; Chu G; Lai G; He R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Dec; 40(12):1455-1460. PubMed ID: 37994123
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case.
    Papamichail M; Eleftheriades A; Manolakos E; Papamichail A; Christopoulos P; Manegold-Brauer G; Eleftheriades M
    BMC Womens Health; 2024 Apr; 24(1):241. PubMed ID: 38622524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.
    Lall M; Thakur S; Puri R; Verma I; Mukerji M; Jha P
    Mol Cytogenet; 2011 Sep; 4():19. PubMed ID: 21936942
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage.
    Lee JM; Shin SY; Kim GW; Kim WJ; Wie JH; Hong S; Kang D; Choi H; Yim J; Kim Y; Kim M; Park IY
    Mol Diagn Ther; 2021 May; 25(3):351-359. PubMed ID: 33792848
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pure Interstitial Trisomy 11q Arising from a Nonrecurrent 11q13.1q22.3 Mosaic Intrachromosomal Duplication in a Patient with Craniofacial Dysmorphism and Genital Anomalies.
    Martínez Anaya D; Juárez-Velázquez MDR; Reyes Ruvalcaba S; Navarrete-Meneses MDP; Salas Labadía C; Lieberman Hernández E; Pérez-Vera P
    Mol Syndromol; 2023 Aug; 14(4):310-321. PubMed ID: 37766825
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP; Wang LK; Chern SR; Wu PS; Ko K; Chen YN; Chen SW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy].
    Lin S; Zhang Z; Wu J; Ji Y; Fang Q; Chen B; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):340-3. PubMed ID: 27264817
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
    Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE
    Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [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]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.