These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
201 related articles for article (PubMed ID: 7333583)
41. Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22; q22; q32) ascertained through a child with partial trisomy 9. Johannisson R; Löhrs U; Passarge E Cytogenet Cell Genet; 1988; 47(3):160-6. PubMed ID: 3378454 [TBL] [Abstract][Full Text] [Related]
42. 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]
43. A reciprocal translocation (X;11) in a female with gonadal dysgenesis. Dorus E; Amarose AP; Tredway DR; Reale FR; Hatch R; Serrano LF Clin Genet; 1979 Oct; 16(4):263-9. PubMed ID: 519895 [TBL] [Abstract][Full Text] [Related]
51. Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation. Leisti JT; Kaback MM; Rimoin DL Am J Hum Genet; 1975 Jul; 27(4):441-53. PubMed ID: 1155455 [TBL] [Abstract][Full Text] [Related]
52. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X. Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871 [TBL] [Abstract][Full Text] [Related]
53. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome. Verellen-Dumoulin C; Freund M; De Meyer R; Laterre C; Frédéric J; Thompson MW; Markovic VD; Worton RG Hum Genet; 1984; 67(1):115-9. PubMed ID: 6745920 [TBL] [Abstract][Full Text] [Related]
54. X;7 translocation in an Indian woman with hypergonadotropic amenorrhea-a case report. Vasu VR; Chandra N; Santhiya ST Genet Test Mol Biomarkers; 2009 Aug; 13(4):533-6. PubMed ID: 19663602 [TBL] [Abstract][Full Text] [Related]
55. Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation. Taysi K; Sparkes RS; O'Brien TJ; Dengler DR J Med Genet; 1982 Apr; 19(2):144-8. PubMed ID: 6210775 [TBL] [Abstract][Full Text] [Related]
56. Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique. Keitges EA; Palmer CG Hum Genet; 1986 Mar; 72(3):231-6. PubMed ID: 3957346 [TBL] [Abstract][Full Text] [Related]
57. X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a female. Turleau C; Niaudet P; Cabanis MO; Plessis G; Cau D; de Grouchy J Clin Genet; 1989 Jun; 35(6):462-6. PubMed ID: 2736795 [TBL] [Abstract][Full Text] [Related]
58. The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility? Karaer K; Ergun MA; Weise A; Ewers E; Liehr T; Kosyakova N; Mkrtchyan H Genet Couns; 2010; 21(4):397-404. PubMed ID: 21290969 [TBL] [Abstract][Full Text] [Related]
59. Hypogonadism in a patient with balanced X/18 translocation and pituitary hormone deficiency. Larizza D; Maraschio P; Maghnie M; Sampaolo P Eur J Pediatr; 1993 May; 152(5):424-7. PubMed ID: 8319711 [TBL] [Abstract][Full Text] [Related]
60. Chiasma derived genetic lengths and recombination fractions: a 46, XY, t(9; 10) (p22; q24) reciprocal translocation. Laurie DA; Palmer RW; Hultén MA Ann Hum Genet; 1985 May; 49(2):135-46. PubMed ID: 4073829 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]