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2. [Diagnosis of minor chromosome modifications by molecular cytogenetics]. Taviaux S; Moncla A; Giraud F; Demaille J; Mattei JF; Mattei MG Ann Genet; 1989; 32(4):204-10. PubMed ID: 2610486 [TBL] [Abstract][Full Text] [Related]
3. 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 [TBL] [Abstract][Full Text] [Related]
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; 46(5):524-8. PubMed ID: 8322814 [TBL] [Abstract][Full Text] [Related]
5. [Immunotherapy following habitual abortion in paternal chromosome translocation]. Glaser D; Wank R; Bartsch-Sandhoff M; Pawlowitzki IH Geburtshilfe Frauenheilkd; 1989 Jan; 49(1):58-60. PubMed ID: 2917707 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Chromosomal abnormalities in couples with recurrent abortions. Low PS; Tay JS; Tan MA; Chua TS; Wong HB J Singapore Paediatr Soc; 1989; 31(1-2):72-4. PubMed ID: 2770260 [TBL] [Abstract][Full Text] [Related]
8. Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages. Wang YT; Bajalica S; Han FY; Wang ZC; Bui TH; Xie YG Am J Med Genet; 1994 Sep; 52(3):349-51. PubMed ID: 7810568 [TBL] [Abstract][Full Text] [Related]
9. Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal loss. Multani AS; Radhakrishna U; Sheth FJ; Shah VC; Chinoy NJ Ann Genet; 1992; 35(2):105-9. PubMed ID: 1524406 [TBL] [Abstract][Full Text] [Related]
10. De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter. Timár L; Béres J; Kosztolányi G; Németh I Hum Genet; 1991 Feb; 86(4):421. PubMed ID: 1999348 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18. Lee MH; Park SY; Kim YM; Kim JM; Han JY; Kim MY; Ryu HM Prenat Diagn; 2002 Feb; 22(2):102-4. PubMed ID: 11857612 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection. Benn PA; Hsu LY; Verma RS; Alonso ML; Reich E; Wishnick M Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Trisomy 18 and a constitutional maternal translocation (2;18). Teshima IE; Winsor EJ; Van Allen MI Am J Med Genet; 1992 Jul; 43(4):759-61. PubMed ID: 1621770 [TBL] [Abstract][Full Text] [Related]
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17. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18. Chen CP; Lin CC; Su YN; Tsai FJ; Chen JT; Chern SR; Lee CC; Town DD; Chen LF; Wu PC; Wang W Taiwan J Obstet Gynecol; 2010 Jun; 49(2):188-91. PubMed ID: 20708526 [TBL] [Abstract][Full Text] [Related]