93 related articles for article (PubMed ID: 18067085)
1. [Establishment of lymphocyte cell lines with abnormal chromosome karyotypes and its application in external quality assesment for chromosome karyotype analysis].
Weng BH; Cai JP; Wang XM; You JF; Jin Y; Wang XH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):689-91. PubMed ID: 18067085
[TBL] [Abstract][Full Text] [Related]
2. [Establishment of permanent lymphoblastoid cell lines of 47 patients with abnormal chromosome karyotype].
Liao SX; Wang YT; Yang YL; Li Y; Huang FF; Hao BT; Wang ZC; Zhu WY; Si YM; Wang YJ
Yi Chuan Xue Bao; 2002 Apr; 29(4):303-6. PubMed ID: 11985262
[TBL] [Abstract][Full Text] [Related]
3. [The cytogenetic characteristics of human B-lymphoblastoid cell lines].
Araviashvili DE; Agrba VZ; Timanovskaia VV; Tsvileneva NN; Mamaeva SE
Tsitologiia; 1994; 36(7):696-700. PubMed ID: 7900210
[TBL] [Abstract][Full Text] [Related]
4. [Establishment of immortalized B-lymphoblastoid cell lines of keloid pedigree and its karyotype analysis].
Song M; Gao JH; Yan X; Liu XJ; Chen Y
Nan Fang Yi Ke Da Xue Xue Bao; 2006 Dec; 26(12):1760-2. PubMed ID: 17259115
[TBL] [Abstract][Full Text] [Related]
5. Detection of human chromosomal abnormalities using a new technique combining 4',6-diamidino-2-phenyl-indole staining and image analysis.
Liu JY; Ji MF; Wang XR; Luo RL; Ren X; Liu M; Wang QK
Clin Genet; 2006 Jan; 69(1):65-71. PubMed ID: 16451138
[TBL] [Abstract][Full Text] [Related]
6. An external quality assessment scheme for prenatal detection of rare chromosomal abnormalities.
Weng B; Li X
Clin Chim Acta; 2012 Nov; 413(21-22):1721-4. PubMed ID: 22789962
[TBL] [Abstract][Full Text] [Related]
7. [Result survey analysis of prenatal chromosome karyotyping in an external quality assessment program].
Wang W; Chen Y; Chen X; Zhong K; He F; Zhang Y; Bao L; Zou L; Wang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):483-6. PubMed ID: 25119916
[TBL] [Abstract][Full Text] [Related]
8. Karyotypes of human T-lymphocyte clones.
Lambert B; Holmberg K; He SH; Einhorn N
IARC Sci Publ; 1988; (89):469-76. PubMed ID: 3264269
[TBL] [Abstract][Full Text] [Related]
9. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
Tönnies H; Pietrzak J; Bocian E; MacDermont K; Kuechler A; Belitz B; Trautmann U; Schmidt A; Schulze B; Rodríguez L; Binkert F; Yardin C; Kosyakova N; Volleth M; Mkrtchyan H; Schreyer I; von Eggeling F; Weise A; Mrasek K; Liehr T
J Histochem Cytochem; 2007 Jun; 55(6):651-60. PubMed ID: 17341473
[TBL] [Abstract][Full Text] [Related]
10. A Novel External Quality Assessment of Chromosomal Karyotype Analysis Based on Chimera Image Assembly.
Weng BH; Shen XY; Xu YL; Ying J; Xu W; Zou DB; He LM; Jin K; Li LJ
Ann Clin Lab Sci; 2020 Sep; 50(5):674-680. PubMed ID: 33067215
[TBL] [Abstract][Full Text] [Related]
11. A case of an intersex horse with 63,X/64,XX/65,XX,del(Y)(q?) karyotype.
Bugno M; Zabek T; Golonka P; Pieńkowska-Schelling A; Schelling C; Słota E
Cytogenet Genome Res; 2008; 120(1-2):123-6. PubMed ID: 18467835
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. External quality assessment of prenatal diagnosis of a rare and subtle chromosomal structural abnormality.
Weng BH; Lu YE; Li X
Eur Rev Med Pharmacol Sci; 2013 Oct; 17(19):2605-8. PubMed ID: 24142606
[TBL] [Abstract][Full Text] [Related]
14. [Simultaneous presence of ins (15;17),t(2;17;20) and trisomy 8 in a patient with acute promyelocytic leukemia].
Bai S; Xue Y; Wu Y; Pan J; Zhang J; Shen J; Wang Y; Qiu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):712-4. PubMed ID: 19065540
[TBL] [Abstract][Full Text] [Related]
15. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
Iourov IY; Vorsanova SG; Liehr T; Monakhov VV; Soloviev IV; Yurov YB
Cytogenet Genome Res; 2008; 121(3-4):302-6. PubMed ID: 18758177
[TBL] [Abstract][Full Text] [Related]
16. The clinical usefulness of chromosome analysis by flow cytometry.
McConnell TS; Cram LS; Baczek N; Fawcett JJ; Luedemann M; Bartholdi MF
Semin Diagn Pathol; 1989 Feb; 6(1):91-107. PubMed ID: 2645627
[TBL] [Abstract][Full Text] [Related]
17. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
18. Novel karyotypes in giant cell-rich lesions of bone.
Gleason BC; Kleinman PK; Debelenko LV; Rahbar R; Gebhardt MC; Perez-Atayde AR
Am J Surg Pathol; 2007 Jun; 31(6):926-32. PubMed ID: 17527082
[TBL] [Abstract][Full Text] [Related]
19. Clonal chromosome abnormalities in two chemodectomas.
Jin Y; Mertens F; Jin C; Wennerberg J; Mandahl N; Heim S; Mitelman F
Genes Chromosomes Cancer; 1996 Mar; 15(3):178-81. PubMed ID: 8721683
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic studies in amenorrhea.
Rajangam S; Nanjappa L
Saudi Med J; 2007 Feb; 28(2):187-92. PubMed ID: 17268694
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]