BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 22419357)

  • 21. Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome.
    Huang XL; Isabel de Michelena M; Leon E; Maher TA; McClure R; Milunsky A
    Clin Genet; 2007 Nov; 72(5):434-40. PubMed ID: 17894838
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter.
    Kirchhoff M; Bisgaard AM; Stoeva R; Dimitrov B; Gillessen-Kaesbach G; Fryns JP; Rose H; Grozdanova L; Ivanov I; Keymolen K; Fagerberg C; Tranebjaerg L; Skovby F; Stefanova M
    Am J Med Genet A; 2009 May; 149A(5):894-905. PubMed ID: 19363806
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3.
    Amor DJ; Voullaire L; Bentley K; Savarirayan R; Choo KH
    Am J Med Genet A; 2005 Mar; 133A(2):151-7. PubMed ID: 15666312
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH.
    Yu S; Barbouth D; Benke PJ; Warburton PE; Fan YS
    Cytogenet Genome Res; 2007; 116(1-2):141-5. PubMed ID: 17268194
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1➔qter in prenatal diagnosis: a case report.
    Altieri V; Capozzi O; Marzano MC; Catapano O; Di Biase I; Rocchi M; De Tollis G
    Mol Cytogenet; 2014; 7(1):69. PubMed ID: 25360155
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
    [TBL] [Abstract][Full Text] [Related]  

  • 27. De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review.
    Syu YM; Ma JY; Ou TH; Lee CL; Lin HY; Lin SP; Lee CJ; Chen CP
    Diagnostics (Basel); 2022 Sep; 12(10):. PubMed ID: 36291995
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.
    Ko JM; Kim JB; Pai KS; Yun JN; Park SJ
    J Korean Med Sci; 2010 Dec; 25(12):1798-801. PubMed ID: 21165297
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
    George-Abraham JK; Zimmerman SL; Hinton RB; Marino BS; Witte DP; Hopkin RJ
    Am J Med Genet A; 2012 Aug; 158A(8):1971-6. PubMed ID: 22711292
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Prenatal diagnosis of a Pallister-Killian syndrome case through analysis of a supernumerary chromosome using single nucleotide polymorphism array].
    Li S; Shen H; Jin Y; Liu X; Song Q; Miao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):682-5. PubMed ID: 27577223
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
    Reddy KS; Sulcova V; Schwartz S; Noble JE; Phillips J; Brasel JA; Huff K; Lin HJ
    Am J Med Genet; 2000 May; 92(1):69-76. PubMed ID: 10797426
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.
    Libotte F; Bizzoco D; Gabrielli I; Mesoraca A; Cignini P; Vitale SG; Marilli I; Gulino FA; Rapisarda AM; Giorlandino C
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome.
    Mathijssen IB; Hoovers JM; Mul AN; Man HY; Ket JL; Hennekam RC
    Am J Med Genet A; 2005 Jul; 136(1):76-80. PubMed ID: 15889415
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
    Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
    Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
    Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
    Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Severe phenotype in a girl with partial tetrasomy 7, karyotype 46,XX,trp(7)(q35q36).
    Lehnen H; Maiwald R; Neyzen S; Kohlhase J; Böhm D; Ritterbach J; Behrend C; Schwennicke G
    Cytogenet Genome Res; 2009; 125(3):248-52. PubMed ID: 19738385
    [TBL] [Abstract][Full Text] [Related]  

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