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 *

183 related articles for article (PubMed ID: 7702096)

  • 1. "Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.
    Wenger SL; Steele MW; Boone LY; Lenkey SG; Cummins JH; Chen XQ
    Am J Med Genet; 1995 Jan; 55(1):47-52. PubMed ID: 7702096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
    Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
    Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of chromosome aberrations in recurrent abortion: a study of 269 balanced translocations.
    Campana M; Serra A; Neri G
    Am J Med Genet; 1986 Jun; 24(2):341-56. PubMed ID: 3717213
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.
    Gijsbers AC; Bosch CA; Dauwerse JG; Giromus O; Hansson K; Hilhorst-Hofstee Y; Kriek M; van Haeringen A; Bijlsma EK; Bakker E; Breuning MH; Ruivenkamp CA
    Eur J Med Genet; 2010; 53(5):227-33. PubMed ID: 20542150
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reproductive risks for translocation carriers: cytogenetic study and analysis of pregnancy outcome in 58 families.
    Neri G; Serra A; Campana M; Tedeschi B
    Am J Med Genet; 1983 Dec; 16(4):535-61. PubMed ID: 6660248
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M; Stembalska A; Schlade K; Zych M
    Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical experience with balanced reciprocal translocations.
    Prieto-Carrasquero M; Rojas-Atencio A; Gonzalez S; Pineda-Del Villar L; Soto M; Quintero M; Miranda LE; Cañizales J
    Genet Couns; 1995; 6(4):349-54. PubMed ID: 8775422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3.
    Pollin TI; Dobyns WB; Crowe CA; Ledbetter DH; Bailey-Wilson JE; Smith AC
    Am J Med Genet; 1999 Aug; 85(4):369-75. PubMed ID: 10398263
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.
    Walker AP; Bocian M
    Am J Med Genet; 1987 May; 27(1):3-22. PubMed ID: 3300332
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic aspects of autosomal fragile sites. Apropos of 40 Cases].
    Guichaoua M; Matteï MG; Matteï JF; Giraud F
    J Genet Hum; 1982 Oct; 30(3):183-97. PubMed ID: 7153767
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Pregnancy outcomes of 194 couples with balanced translocations].
    Zhang YP; Xu JZ; Yin M; Chen MF; Ren DL
    Zhonghua Fu Chan Ke Za Zhi; 2006 Sep; 41(9):592-6. PubMed ID: 17181967
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
    Gajecka M; Glotzbach CD; Jarmuz M; Ballif BC; Shaffer LG
    Eur J Hum Genet; 2006 Dec; 14(12):1255-62. PubMed ID: 16941016
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
    Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
    Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).
    Schinzel A
    Am J Med Genet; 1984 May; 18(1):153-61. PubMed ID: 6430085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B; Kotzot D; Brecevic L; Koehler M; Balmer D; Binkert F; Schinzel A
    Eur J Hum Genet; 1999 Dec; 7(8):873-83. PubMed ID: 10602362
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Balanced reciprocal translocation mosaicism associated with an abnormal phenotype.
    Aughton DJ; AlSaadi AA; Canady AI; Lucas BM
    Am J Med Genet; 1993 Mar; 45(6):721-4. PubMed ID: 8456851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.