105 related articles for article (PubMed ID: 2996350)
1. Minute chromosomes replacing the Y chromosome carry Y-specific sequences by restriction fragment analysis and in situ hybridization.
Münke M; de Martinville B; Lieber E; Francke U
Am J Med Genet; 1985 Oct; 22(2):361-74. PubMed ID: 2996350
[TBL] [Abstract][Full Text] [Related]
2. Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes.
Müller U; Latt SA; Donlon T
Am J Med Genet; 1987 Oct; 28(2):393-401. PubMed ID: 2827475
[TBL] [Abstract][Full Text] [Related]
3. Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.
Ogata T; Wakui K; Kosho T; Muroya K; Yamanouchi Y; Takano T; Fukushima Y; Rappold G; Suzuki Y
Am J Med Genet; 2000 Jun; 92(4):256-9. PubMed ID: 10842291
[TBL] [Abstract][Full Text] [Related]
4. A molecular method for detecting the presence of the human Y chromosome.
Friesen H; Nishioka Y
Am J Med Genet; 1984 Jun; 18(2):289-94. PubMed ID: 6087662
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Breakpoint of a Y chromosome pericentric inversion in the DAZ gene area. A case report.
Causio F; Canale D; Schonauer LM; Fischetto R; Leonetti T; Archidiacono N
J Reprod Med; 2000 Jul; 45(7):591-4. PubMed ID: 10948474
[TBL] [Abstract][Full Text] [Related]
7. [Intra-individual polymorphism of human Y chromosome as a result of deletion in the heterochromatin region].
Nazarenko SA; Nazarenko LP; Baranova VA
Genetika; 1987 May; 23(5):918-21. PubMed ID: 3623089
[TBL] [Abstract][Full Text] [Related]
8. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.
Valetto A; Bertini V; Rapalini E; Baldinotti F; Di Martino D; Simi P
Fertil Steril; 2004 May; 81(5):1388-90. PubMed ID: 15136108
[TBL] [Abstract][Full Text] [Related]
9. The use of fluorescence in-situ hybridisation to clarify abnormal Y chromosomes in two infertile men.
Smith A; Conway A; Robson L
Med J Aust; 1994 May; 160(9):545, 548-9, 552. PubMed ID: 8164552
[TBL] [Abstract][Full Text] [Related]
10. Mosaic ring Y chromosome in two normal healthy men with azoospermia.
Bertini V; Canale D; Bicocchi MP; Simi P; Valetto A
Fertil Steril; 2005 Dec; 84(6):1744. PubMed ID: 16359976
[TBL] [Abstract][Full Text] [Related]
11. Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
Pezzolo A; Perroni L; Gimelli G; Arslanian A; Porta S; Gandullia P; Gandullia E
Ann Genet; 1993; 36(2):121-5. PubMed ID: 8215218
[TBL] [Abstract][Full Text] [Related]
12. Preparative dual-beam sorting of the human Y chromosome and in situ hybridization of cloned DNA probes.
Cremer C; Rappold G; Gray JW; Müller CR; Ropers HH
Cytometry; 1984 Nov; 5(6):572-9. PubMed ID: 6549159
[TBL] [Abstract][Full Text] [Related]
13. A long-range restriction map of deletion interval 6 of the human Y chromosome: a region frequently deleted in azoospermic males.
Yen PH
Genomics; 1998 Nov; 54(1):5-12. PubMed ID: 9806824
[TBL] [Abstract][Full Text] [Related]
14. Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.
Park SJ; Jeong SY; Kim HJ
Cancer Genet Cytogenet; 2006 Apr; 166(1):56-64. PubMed ID: 16616112
[TBL] [Abstract][Full Text] [Related]
15. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
16. [Molecular detection of chromosome Y DNA sequences in patients with Turner's syndrome].
López López M; Torres Maldonado LC; Pablo Méndez J; Cervantes Peredo A; Canto Cetina P; Pérez-Palacios G; Kofman-Alfaro S
Rev Invest Clin; 1993; 45(3):233-9. PubMed ID: 8210766
[TBL] [Abstract][Full Text] [Related]
17. Giemsa-11 technique elucidating three structurally altered nonfluorescent Y chromosomes: r (Y), idic (Yp), dir tan dup (Yp).
Kosztolányi G
Ann Genet; 1988; 31(4):235-40. PubMed ID: 3265307
[TBL] [Abstract][Full Text] [Related]
18. Analysis for microdeletions of Y chromosome in a single spermatozoon from a man with severe oligozoospermia.
Komori S; Nakata Y; Sakata K; Kato H; Koyoma K
J Hum Genet; 2001; 46(2):76-9. PubMed ID: 11281416
[TBL] [Abstract][Full Text] [Related]
19. [Strategies for detecting restriction polymorphisms of Y chromosome sequences].
Ngo KY; Lucotte G
Ann Genet; 1986; 29(2):88-92. PubMed ID: 2876675
[TBL] [Abstract][Full Text] [Related]
20. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).
Kocova M; Siegel SF; Wenger SL; Lee PA; Nalesnik M; Trucco M
Am J Med Genet; 1995 Feb; 55(4):483-8. PubMed ID: 7762591
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]