126 related articles for article (PubMed ID: 12503194)
21. Case of (Y;1) familial translocation.
Teyssier M; Rafat A; Pugeat M
Am J Med Genet; 1993 May; 46(3):339-40. PubMed ID: 8488881
[TBL] [Abstract][Full Text] [Related]
22. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
Qumsiyeh MB; Dalton JD; Gordon PL; Wilroy RS; Tharapel AT
Am J Med Genet; 1992 Jan; 42(1):109-11. PubMed ID: 1308348
[TBL] [Abstract][Full Text] [Related]
23. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
Cheng DH; Tan YQ; Di YF; Li LY; Lu GX
Fertil Steril; 2009 Aug; 92(2):828.e3-6. PubMed ID: 19524892
[TBL] [Abstract][Full Text] [Related]
24. An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies.
Cui YX; Xia XY; Pan LJ; Wang YH; Yao B; Huang YF
Fertil Steril; 2007 Dec; 88(6):1676.e7-11. PubMed ID: 17482602
[TBL] [Abstract][Full Text] [Related]
25. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
26. [Genetic analysis of a complex chromosome rearrangement involving two chromosomes and four breakpoints in an azoospermic man].
Luo YQ; Shen M; Qian YL; Chen YL; Xu CM; Jin F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):200-2. PubMed ID: 19350516
[TBL] [Abstract][Full Text] [Related]
27. Pure partial trisomy 7q: two new patients and review.
Rodríguez L; López F; Paisán L; de la Red Mdel M; Ruiz AM; Blanco M; Antelo Cortizas J; Martínez-Frías ML
Am J Med Genet; 2002 Nov; 113(2):218-24. PubMed ID: 12407716
[TBL] [Abstract][Full Text] [Related]
28. A prevalent Y;15 translocation in the Ethiopian Beta Israel community in Israel.
Chen-Shtoyerman R; Josefsberg Ben-Yehoshua S; Nissani R; Rosensaft J; Appelman Z
Cytogenet Genome Res; 2012; 136(3):171-4. PubMed ID: 22327880
[TBL] [Abstract][Full Text] [Related]
29. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
30. Infertility in a man with oligoasthenoteratozoospermia associated with nonrobertsonian translocation t(9;15)(p10;q10).
Aydos SE; Tükün A
Fertil Steril; 2006 Oct; 86(4):1001.e7-9. PubMed ID: 17027368
[TBL] [Abstract][Full Text] [Related]
31. Chromosome analysis of epididymal and testicular spermatozoa in patients with azoospermia.
Burrello N; Calogero AE; De Palma A; Grazioso C; Torrisi C; Barone N; Pafumi C; D'Agata R; Vicari E
Eur J Hum Genet; 2002 Jun; 10(6):362-6. PubMed ID: 12080387
[TBL] [Abstract][Full Text] [Related]
32. Male infertility: Y-chromosome deletion and testicular aetiology in cases of azoo-/oligospermia.
Singh K; Raman R
Indian J Exp Biol; 2005 Nov; 43(11):1088-92. PubMed ID: 16313071
[TBL] [Abstract][Full Text] [Related]
33. Azoospermic male with a balanced Y-autosome translocation.
Matsuda T; Hayashi K; Nonomura M; Yamamoto S; Yoshida O
Urol Int; 1989; 44(1):43-6. PubMed ID: 2665261
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. Alternative centromeric inactivation in a pseudodicentric t(Y;13)(q12;p11.2) translocation chromosome associated with extreme oligozoospermia.
Siffroi JP; Benzacken B; Angelopoulou R; Le Bourhis C; Berthaut I; Kanafani S; Smahi A; Wolf JP; Dadoune JP
J Med Genet; 2001 Nov; 38(11):802-6. PubMed ID: 11732493
[No Abstract] [Full Text] [Related]
37. Prenatal detection of a de novo Yqh-acrocentric translocation.
Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
[TBL] [Abstract][Full Text] [Related]
38. Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2).
Cantú JM; Díaz M; Möller M; Jiménez-Sáinz M; Sandoval L; Vaca G; Rivera H
Am J Med Genet; 1985 Apr; 20(4):677-84. PubMed ID: 3993688
[TBL] [Abstract][Full Text] [Related]
39. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
[TBL] [Abstract][Full Text] [Related]
40. Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia.
Buijs A; Terhal PA; Thunnissen PL
Cancer Genet Cytogenet; 2006 Jul; 168(1):80-2. PubMed ID: 16772126
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
