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 *

300 related articles for article (PubMed ID: 15065104)

  • 21. Prenatal diagnosis and molecular cytogenetic characterization of an unusual complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI).
    Trimborn M; Liehr T; Belitz B; Pfeiffer L; Varon R; Neitzel H; Tönnies H
    J Histochem Cytochem; 2005 Mar; 53(3):351-4. PubMed ID: 15750017
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of supernumerary ring chromosome 1: case report and review of the literature.
    Wray AM; Dennis TR; Ghidini A; Gorman B; Haddad BR; Meck JM
    Genet Couns; 2007; 18(2):233-41. PubMed ID: 17710876
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
    Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
    Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities.
    Müller-Navia J; Nebel A; Oehler D; Theile U; Zabel B; Schleiermacher E
    Prenat Diagn; 1996 Oct; 16(10):915-22. PubMed ID: 8938060
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
    Chen CP; Liu FF; Jan SW; Yang YC; Lan CC
    Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
    Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
    Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report.
    Joly-Helas G; de La Rochebrochard C; Mousset-Siméon N; Moirot H; Tiercin C; Romana SP; Le Caignec C; Clavier B; Macé B; Rives N
    Hum Reprod; 2007 May; 22(5):1292-7. PubMed ID: 17283038
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.
    Aslan H; Karaman B; Yildirim G; Ceylan Y
    Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308
    [TBL] [Abstract][Full Text] [Related]  

  • 32. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P; Buldrini B; Aiello V; Gruppioni R; Bonfatti A; Venti G; Ferlini A; Sensi A; Calzolari E; Donti E
    Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?
    Karmous-Benailly H; Tabet AC; Thaly A; Dupuy O; Huten Y; Luton D; Baumann C; Delezoide AL
    Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD; Musci TJ
    Prenat Diagn; 2001 Mar; 21(3):171-5. PubMed ID: 11260602
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
    Kanafani S; Aboura A; Pipiras E; Carbillon L; Tabet AC; Largillière C; Garel C; Gressens P; Bucourt M; Cedrin-Durnerin I; Lachassinne E; Roumegoux C; Uzan M; Hugues JN; Wolf JP; Benzacken B
    Prenat Diagn; 2007 Mar; 27(3):279-84. PubMed ID: 17269127
    [TBL] [Abstract][Full Text] [Related]  

  • 37. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review.
    Batanian JR; Eswara MS
    Am J Med Genet; 1998 Jun; 78(1):44-51. PubMed ID: 9637422
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
    Fryns JP; Kleczkowska A
    Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21).
    Witters I; Balikova I; Cannie M; Devriendt K; De Catte L; Fryns JP
    Genet Couns; 2008; 19(4):443-6. PubMed ID: 19239091
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.