137 related articles for article (PubMed ID: 8362916)
1. Moving satellites and unstable chromosome translocations: clinical and cytogenetic implications.
Farrell SA; Winsor EJ; Markovic VD
Am J Med Genet; 1993 Jul; 46(6):715-20. PubMed ID: 8362916
[TBL] [Abstract][Full Text] [Related]
2. [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
Solov'ev IV; Iurov IuB; Vorsanova SG; Marcais B; Rogaev EI; Kapanadze BI; Brodianskiĭ VM; Iankovskiĭ NK; Roizes G
Genetika; 1998 Nov; 34(11):1470-9. PubMed ID: 10096024
[TBL] [Abstract][Full Text] [Related]
3. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
[TBL] [Abstract][Full Text] [Related]
4. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
Pierluigi M; Battaglia P; Perfumo C; Baroncini A; Bricarelli FD
Ann Genet; 1997; 40(2):99-103. PubMed ID: 9259956
[TBL] [Abstract][Full Text] [Related]
5. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
[TBL] [Abstract][Full Text] [Related]
6. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
[TBL] [Abstract][Full Text] [Related]
7. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
[TBL] [Abstract][Full Text] [Related]
8. Loss of 17p is a major consequence of whole-arm chromosome translocations in hematologic malignancies.
Adeyinka A; Wei S; Sanchez J
Cancer Genet Cytogenet; 2007 Mar; 173(2):136-43. PubMed ID: 17321329
[TBL] [Abstract][Full Text] [Related]
9. A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: further studies on Robertsonian translocations.
Kalitsis P; Earle E; Vissel B; Shaffer LG; Choo KH
Genomics; 1993 Apr; 16(1):104-12. PubMed ID: 8486347
[TBL] [Abstract][Full Text] [Related]
10. Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.
Sullivan BA; Jenkins LS; Karson EM; Leana-Cox J; Schwartz S
Am J Hum Genet; 1996 Jul; 59(1):167-75. PubMed ID: 8659523
[TBL] [Abstract][Full Text] [Related]
11. Dual-color fish analysis of breakpoints on Robertsonian translocations.
Takahashi Y; Fujita H; Nakamura Y; Kurahashi H
Jpn J Hum Genet; 1997 Dec; 42(4):517-23. PubMed ID: 9560951
[TBL] [Abstract][Full Text] [Related]
12. [Cytogenetic and molecular genetic study on a female with complex translocation of t(Y;15) and t(14;21)].
Shi Y; Ma S; Wang Y; Gao C; Ye L; Cheng Z
Yi Chuan Xue Bao; 1993; 20(6):488-92. PubMed ID: 8179934
[TBL] [Abstract][Full Text] [Related]
13. Promiscuous translocations of chromosome arm 17q in human neuroblastomas.
Lastowska M; Roberts P; Pearson AD; Lewis I; Wolstenholme J; Bown N
Genes Chromosomes Cancer; 1997 Jul; 19(3):143-9. PubMed ID: 9218994
[TBL] [Abstract][Full Text] [Related]
14. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
Barbi G; Kennerknecht I; Klett C
Am J Med Genet; 1992 Jul; 43(4):722-5. PubMed ID: 1621764
[TBL] [Abstract][Full Text] [Related]
15. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
De Pater JM; Van Tintelen JP; Stigter R; Brouwers HA; Scheres JM
Genet Couns; 2000; 11(3):241-7. PubMed ID: 11043432
[TBL] [Abstract][Full Text] [Related]
16. Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
Starke H; Mrasek K; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):359-60. PubMed ID: 15750019
[TBL] [Abstract][Full Text] [Related]
17. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
Alves C; Carvalho F; Cremades N; Sousa M; Barros A
Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
[TBL] [Abstract][Full Text] [Related]
18. Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization.
Gravholt CH; Friedrich U; Caprani M; Jørgensen AL
Genomics; 1992 Dec; 14(4):924-30. PubMed ID: 1478673
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
[TBL] [Abstract][Full Text] [Related]
20. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
