BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 10210132)

  • 1. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.
    Faivre L; Morichon-Delvallez N; Viot G; Larget-Piet A; Narcy F; Turleau C; Pinson MP; Dumez Y; Munnich A; Vekemans M
    Prenat Diagn; 1999 Mar; 19(3):282-6. PubMed ID: 10210132
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of interstitially satellited 6p.
    Chen CP; Chern SR; Lee CC; Chen WL; Wang W
    Prenat Diagn; 2004 Jun; 24(6):430-3. PubMed ID: 15229841
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG; Moerman P; Fryns JP
    Genet Couns; 1996; 7(4):313-9. PubMed ID: 8985736
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis.
    Ogur G; Hayez F; Herinckx A; Van Regemorter N; Vamos E
    J Genet Hum; 1988 Aug; 36(4):323-9. PubMed ID: 3221208
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Family with partial monosomy 10p and trisomy 10p.
    Hon E; Chapman C; Gunn TR
    Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).
    Martin-Denavit T; Attia-Sobol J; Theuil J; Abel-Lablanche K; Boggio D; Teyssier M; Till M; Champion F; Vitrey D; Plauchu H
    Prenat Diagn; 2002 Jun; 22(6):487-9. PubMed ID: 12116308
    [No Abstract]   [Full Text] [Related]  

  • 10. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
    Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
    Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
    Sarri C; Douzgou S; Gyftodimou Y; Tümer Z; Ravn K; Pasparaki A; Sarafidou T; Kontos H; Kokotas H; Karadima G; Grigoriadou M; Pandelia E; Theodorou V; Moschonas NK; Petersen MB
    Am J Med Genet A; 2011 Nov; 155A(11):2841-54. PubMed ID: 21964744
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
    Migliori MV; Pettinari A; Ciaschini AM; Piermattei P; Pigliapoco F; Discepoli G
    Prenat Diagn; 2004 Apr; 24(4):290-2. PubMed ID: 15065104
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
    Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
    Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
    Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
    Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Centromeric alpha-satellite DNA break in reciprocal translocations.
    Wang JC; Hajianpour A; Habibian R
    Cytogenet Genome Res; 2009; 125(4):329-33. PubMed ID: 19864896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Nucleolus organizer region--centromere translocation].
    de Blois MC; Rethoré MO; Lejeune J
    Ann Genet; 1989; 32(2):106-8. PubMed ID: 2757357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 20p from maternal translocation and anencephaly. Case report and genetic review.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López Pajares I
    Ann Genet; 1989; 32(4):247-9. PubMed ID: 2610493
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.