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871 related items for PubMed ID: 18990986

  • 1. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D.
    Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
    [Abstract] [Full Text] [Related]

  • 2. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O, Tastemir D.
    Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035
    [Abstract] [Full Text] [Related]

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  • 4. Reproductive risk in mating between two translocation carriers: case report and review of the literature.
    Tsuji K, Narahara K, Yokoyama Y, Ninomiya S, Yonesawa S, Hiramatsu Y, Masaoka H, Kudo N, Seino Y.
    Am J Med Genet; 1993 Jun 15; 46(5):524-8. PubMed ID: 8322814
    [Abstract] [Full Text] [Related]

  • 5. [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 15; 31(2):125-31. PubMed ID: 15473301
    [Abstract] [Full Text] [Related]

  • 6. Inheritance of a Chromosome 3 and 21 Translocation in the Fetuses, with One also Having Trisomy 21, in Three Pregnancies in One Family.
    Pazarbasi A, Demirhan O, Alptekin D, Ozgunen F, Ozpak L, Yilmaz M, Nazlican E, Tanriverdi N, Luleyap U, Gümürdülü D.
    Balkan J Med Genet; 2013 Dec 15; 16(2):91-6. PubMed ID: 24778571
    [Abstract] [Full Text] [Related]

  • 7. Reproductive risk of t(13q14q) carriers: case report and review.
    Harris DJ, Hankins L, Begleiter ML.
    Am J Med Genet; 1979 Dec 15; 3(2):175-81. PubMed ID: 157697
    [Abstract] [Full Text] [Related]

  • 8. Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report.
    Wiland E, Hobel CJ, Hill D, Kurpisz M.
    Prenat Diagn; 2008 Jan 15; 28(1):36-41. PubMed ID: 18186141
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 16(4):535-61. PubMed ID: 6660248
    [Abstract] [Full Text] [Related]

  • 10. Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling.
    Demirhan O, Ozcan K, Taştemir D, Demir C, Tunç E, Solğun HA, Güzel AI.
    Fertil Steril; 2008 Jan 15; 89(1):228.e1-6. PubMed ID: 17880960
    [Abstract] [Full Text] [Related]

  • 11. 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 Jan 15; 46(4):419-21. PubMed ID: 16278518
    [Abstract] [Full Text] [Related]

  • 12. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT.
    Ann Genet; 2004 Jan 15; 47(1):11-28. PubMed ID: 15050871
    [Abstract] [Full Text] [Related]

  • 13. Sotos syndrome with a balanced reciprocal translocation t(2;12)(q33.3;q15).
    Tamaki K, Horie K, Go T, Okuno T, Mikawa H, Hua ZY, Abe T.
    Ann Genet; 1989 Jan 15; 32(4):244-6. PubMed ID: 2610492
    [Abstract] [Full Text] [Related]

  • 14. The analysis of meiotic segregation patterns and aneuploidy in the spermatozoa of father and son with translocation t(4;5)(p15.1;p12) and the prediction of the individual probability rate for unbalanced progeny at birth.
    Wiland E, Midro AT, Panasiuk B, Kurpisz M.
    J Androl; 2007 Jan 15; 28(2):262-72. PubMed ID: 17021336
    [Abstract] [Full Text] [Related]

  • 15. Recurrent abortions and down syndrome resulting from Robertsonian translocation 21q; 21q.
    Kolgeci S, Azemi M, Ahmeti H, Dervishi Z, Sopjani M, Kolgeci J.
    Med Arch; 2012 Jan 15; 66(5):350-2. PubMed ID: 23097978
    [Abstract] [Full Text] [Related]

  • 16. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984 Jan 15; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 17. [Translocation (X; Y) and genetic counseling].
    Mugneret F, Sidaner I, Nivelon-Chevallier A, Koening M, Parise F, Turc-Carel C.
    J Genet Hum; 1988 Jan 15; 36(1-2):93-7. PubMed ID: 3379384
    [Abstract] [Full Text] [Related]

  • 18. 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 Jan 15; 17(3):315-20. PubMed ID: 17100200
    [Abstract] [Full Text] [Related]

  • 19. Segregation of acrocentric chromosome association in familial dicentric Robertsonian translocation t(14p;22p), aneuploidy (trisomy-21) and heteromorphism.
    Murthy DS, Sundareshan TS, Farag TI, al-Awadi SA, al-Othman SA.
    Indian J Exp Biol; 1990 Jun 15; 28(6):511-5. PubMed ID: 2144840
    [Abstract] [Full Text] [Related]

  • 20. [Double translocation 46, XX, t(2; 5), t(2; 18) with major reproduction problems].
    Sidaner I, Nivelon-Chevallier A, Mugneret F, Turc-Carel C.
    J Genet Hum; 1988 Jan 15; 36(1-2):89-92. PubMed ID: 3379383
    [Abstract] [Full Text] [Related]

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