BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 22086126)

  • 1. A new case of pure partial 7q duplication.
    Alfonsi M; Palka C; Morizio E; Gatta V; Franchi S; Guanciali Franchi P; Zori R; Calabrese G; Palka G; Chiarelli F
    Cytogenet Genome Res; 2012; 136(1):1-5. PubMed ID: 22086126
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy of 7q: case report and literature review.
    Scelsa B; Bedeschi FM; Guerneri S; Lalatta F; Introvini P
    J Child Neurol; 2008 May; 23(5):572-9. PubMed ID: 18056692
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A family with an inverted tandem duplication 5q22.1q23.2.
    Schmidt T; Bartels I; Liehr T; Burfeind P; Zoll B; Shoukier M
    Cytogenet Genome Res; 2013; 139(1):65-70. PubMed ID: 23051634
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.
    Frühmesser A; Erdel M; Duba HC; Fauth C; Amberger A; Utermann G; Zschocke J; Kotzot D
    Eur J Med Genet; 2013 Jul; 56(7):383-8. PubMed ID: 23608969
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
    Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
    Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo dup(7)(q21q22.2) and cytogenetics of 7q21q34 duplications.
    Rivera H
    Genet Couns; 2013; 24(3):291-7. PubMed ID: 24341144
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposis.
    Lukusa T; Fryns JP
    Genet Couns; 2010; 21(1):25-34. PubMed ID: 20420026
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Concurrence of inv(7)(q11.2q32) and del(8)(p23.1) in a girl with congenital microcephaly, hypotonia, developmental delay, strabismus, hypernatremia, hypermagnesemia and deafness.
    Mahjoubi F; Nasiri F; Razazian F
    Genet Couns; 2012; 23(3):397-404. PubMed ID: 23072189
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
    Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
    Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
    Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
    Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
    Tan EC; Lim E; Cham B; Knight L; Ng I
    Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report.
    Ruiz-Botero F; Pachajoa H
    J Med Case Rep; 2016 Jul; 10():204. PubMed ID: 27459995
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
    Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
    Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
    Chen CP; Lin SP; Chen MR; Su YN; Chern SR; Liu YP; Su JW; Lee MS; Wang W
    Genet Couns; 2012; 23(3):405-13. PubMed ID: 23072190
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
    Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
    Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders.
    Milani D; Bedeschi MF; Iascone M; Chiarelli G; Cerutti M; Menni F
    Cytogenet Genome Res; 2012; 136(3):167-70. PubMed ID: 22398643
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.