BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

454 related articles for article (PubMed ID: 19480332)

  • 1. A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation.
    Türköver BB; Sayar C; Toksoy G; Elçioğlu N
    Turk J Pediatr; 2009; 51(2):174-9. PubMed ID: 19480332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T; Yu P; Tagle DA; Xia J
    Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial duplication for the short arm of chromosome 2 : the 2p23 to pter syndrome.
    Rosenfeld W; Verma RS; Jhaveri R; Dosik H; Evans H
    Ann Genet; 1982; 25(1):28-31. PubMed ID: 6979296
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial deletion of distal 17q.
    Bridge J; Sanger W; Mosher G; Buehler B; Nelson R; Welsh M; Newland J; Kafka M
    Am J Med Genet; 1985 Jun; 21(2):225-9. PubMed ID: 4014309
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).
    Krüger G; Götz J; Kvist U; Dunker H; Erfurth F; Pelz L; Zech L
    Am J Med Genet; 1989 Mar; 32(3):411-6. PubMed ID: 2729360
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.
    Eid MO; Eid MM; Kamel AK; El-Ruby M; Abdel-Salam GM
    Genet Couns; 2015; 26(2):153-61. PubMed ID: 26349184
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
    Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A new case of a severe clinical phenotype of the cat-eye syndrome.
    Denavit TM; Malan V; Grillon C; Sanlaville D; Ardalan A; Jacquemont ML; Burglen L; Taillemite JL; Portnoi MF
    Genet Couns; 2004; 15(4):443-8. PubMed ID: 15658620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a fetus with partial trisomy 7p.
    Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
    Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal detection of deletion 6q13q15 in a complex karyotype.
    Yu M; Obringer AC; Fowler MH; Hummel M; Wenger SL
    Prenat Diagn; 2005 Dec; 25(12):1084-7. PubMed ID: 16231325
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Emerging phenotype of duplication (7p): a report of three cases and review of the literature.
    Milunsky JM; Wyandt HE; Milunsky A
    Am J Med Genet; 1989 Jul; 33(3):364-8. PubMed ID: 2679090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
    Senses DA; Silan F; Uzun H; Alagöz D; Zafer C; Kocabay K; Karaüzüm SB; Cetin Z
    Genet Couns; 2007; 18(2):163-70. PubMed ID: 17710868
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B; Moore R; Mohandas T
    Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.