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.
248 related articles for article (PubMed ID: 6460105)
1. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally. Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis. Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273 [TBL] [Abstract][Full Text] [Related]
3. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation. Cantu JM; Hernandez A; Plascencia L; Vaca G; Moller M; Rivera H Ann Genet; 1980; 23(3):183-6. PubMed ID: 6448566 [TBL] [Abstract][Full Text] [Related]
4. Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3. Putra M; Surti U; Hu J; Steele D; Clemens M; Saller DN; Yatsenko SA; Rajkovic A Am J Med Genet A; 2017 Dec; 173(12):3153-3157. PubMed ID: 29048729 [TBL] [Abstract][Full Text] [Related]
5. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter). Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269 [TBL] [Abstract][Full Text] [Related]
6. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis]. Zolotukhina TV; Rozovskiĭ IS; Bartseva OB; Vakhlamova IV; Bubnova NI Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355 [TBL] [Abstract][Full Text] [Related]
7. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22). Rivera H; Rivas F; Plascencia L; Cantú JM Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704 [TBL] [Abstract][Full Text] [Related]
8. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings. Beneck D; Greco MA; Wolman SR; McMorrow LE; Jansen V; Cason J J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557 [TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report. Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098 [TBL] [Abstract][Full Text] [Related]
10. [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; 18(3):223-8. PubMed ID: 6235655 [TBL] [Abstract][Full Text] [Related]
11. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20. Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping. Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296 [TBL] [Abstract][Full Text] [Related]
13. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation. Duckett DP; Porter HJ; Young ID Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408 [TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS). Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689 [TBL] [Abstract][Full Text] [Related]
15. Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5). Gilgenkrantz S; Dulucq P; Bresson JL; Gouget A; Pernot C; Gregoire MJ J Med Genet; 1981 Dec; 18(6):465-9. PubMed ID: 7334508 [TBL] [Abstract][Full Text] [Related]
17. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24). Balci S; Aypar E; Beksaç MS; Bartsch O Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409 [TBL] [Abstract][Full Text] [Related]
18. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18. Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082 [TBL] [Abstract][Full Text] [Related]