393 related articles for article (PubMed ID: 11517768)
1. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
Karamysheva TV; Matveeva VG; Shorina AP; Rubtsov NB
Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
3. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
[TBL] [Abstract][Full Text] [Related]
4. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
5. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
Martínez A; Ramos S; González-del Angel A; Alcántara MA; Molina B; Carnevale A
Rev Invest Clin; 2007; 59(6):444-8. PubMed ID: 18402336
[TBL] [Abstract][Full Text] [Related]
6. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
7. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
8. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
[TBL] [Abstract][Full Text] [Related]
9. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
11. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
[TBL] [Abstract][Full Text] [Related]
12. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
Bregant L; Gersak K; Veble A
Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
[TBL] [Abstract][Full Text] [Related]
13. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetic and molecular analysis in trisomy 12p.
Allen TL; Brothman AR; Carey JC; Chance PF
Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
[TBL] [Abstract][Full Text] [Related]
15. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
[TBL] [Abstract][Full Text] [Related]
16. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
Mark HF; Wyandt H; Pan A; Milunsky JM
Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
[TBL] [Abstract][Full Text] [Related]
19. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
Qiu H; Xue Y; Zhang J; Pan J; Dai H; Wu Y; Wang Y; Chen S; Wu D
Exp Hematol; 2008 Nov; 36(11):1487-95. PubMed ID: 18715689
[TBL] [Abstract][Full Text] [Related]
20. Novel translocation t(3;11)(p21;q24) in multiple myeloma characterised by FISH.
Smith A; de Lambert R; Robson L
Ann Genet; 1999; 42(4):221-4. PubMed ID: 10674162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
