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 *

159 related articles for article (PubMed ID: 21815264)

  • 21. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
    Mrasek K; Starke H; Liehr T
    J Histochem Cytochem; 2005 Mar; 53(3):367-70. PubMed ID: 15750022
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: characterization and evaluation of the aberrations.
    Schwanitz G; Hagh JK; Rad IA; Omrani MD; Gamerdinger U; Schubert R; Elbracht M; Eggermann T; Eggermann K; Spengler S; Schüler H; Gogiel M
    Am J Med Genet A; 2014 Mar; 164A(3):736-40. PubMed ID: 24357605
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
    Chen CP; Chern SR; Chen YN; Chen SW; Wu PS; Yang CW; Lee CC; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
    [TBL] [Abstract][Full Text] [Related]  

  • 24. PARTIAL TRISOMY 5p12-q 11.2 RESULTING FROM A MARKER CHROMOSOME: A NEW CASE REPORT WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER.
    Erdem HB; Sahin I; Tasdemir S; Tatar A
    Genet Couns; 2016; 27(3):295-303. PubMed ID: 30204959
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14.
    Velissariou V; Sachinidi F; Christopoulou S; Florentin L; Liehr T; Efthymiadou A; Angelopoulou E; Chrysis D; Stefanou EG
    Cytogenet Genome Res; 2020; 160(11-12):664-670. PubMed ID: 33202412
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3.
    Chen CP; Ko TM; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):864-868. PubMed ID: 31759544
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation?
    Liehr T; Kosyakova N
    Tsitologiia; 2013; 55(3):165-6. PubMed ID: 23795458
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Clinical and genetic analysis of a rare case with mosaic partial trisomy 5p syndrome].
    He T; Liu Y; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):1032-1035. PubMed ID: 32820524
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification and characterization of a complex pure mosaic of small supernumerary marker chromosomes involving 11p11.12 → q12.1 and 19p12 → q12 regions in a child featuring multiple congenital anomalies.
    Fei X; Qi M; Zhao Y; Li-Ling J
    Am J Med Genet A; 2011 Dec; 155A(12):3116-21. PubMed ID: 22069249
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature.
    Shao HY; Miao ZY; Liu XY; Hou XF; Wu H
    Taiwan J Obstet Gynecol; 2020 Mar; 59(2):323-326. PubMed ID: 32127158
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP; Chen M; Su YN; Huang JP; Chern SR; Wu PS; Su JW; Chang SP; Chen YT; Lee CC; Chen LF; Pan CW; Wang W
    Gene; 2013 Oct; 529(1):169-75. PubMed ID: 23933412
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells.
    Tsai MC; Cheng HY; Su MT; Chen M; Kuo PL
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):598-601. PubMed ID: 25510708
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.
    Chen CP; Chen M; Wang PT; Chern SR; Chen SW; Lai ST; Wu PS; Chang SP; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):394-397. PubMed ID: 28600058
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
    Chen CP; Chen M; Wu CH; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):554-557. PubMed ID: 28805618
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.
    Melo JB; Backx L; Vermeesch JR; Santos HG; Sousa AC; Kosyakova N; Weise A; von Eggeling F; Liehr T; Carreira IM
    J Appl Genet; 2011 May; 52(2):193-200. PubMed ID: 21437654
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype.
    Sung PL; Chang SP; Wen KC; Chang CM; Yang MJ; Chen LC; Chao KC; Huang CY; Li YC; Lin CC
    Am J Med Genet A; 2009 Dec; 149A(12):2768-74. PubMed ID: 19921638
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH.
    Wood E; Dowey S; Saul D; Cain C; Rossiter J; Blakemore K; Stetten G
    Am J Med Genet A; 2008 Mar; 146A(6):764-9. PubMed ID: 18241063
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.
    Lebedev IN; Karamysheva TV; Elisaphenko EA; Makunin AI; Zhigalina DI; Lopatkina ME; Drozdov GV; Cheremnykh AD; Torkhova NB; Seitova GN; Vasilyev SA; Kashevarova AA; Nazarenko LP; Rubtsov NB
    Biomedicines; 2021 Aug; 9(8):. PubMed ID: 34440234
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes.
    Cheng D; Yuan S; Yi D; Luo K; Xu F; Gong F; Lu C; Lu G; Lin G; Tan YQ
    J Assist Reprod Genet; 2019 Dec; 36(12):2533-2539. PubMed ID: 31720922
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.