195 related articles for article (PubMed ID: 1583640)
21. Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocation.
Gabriel-Robez O; Rumpler Y; Ratomponirina C; Petit C; Levilliers J; Croquette MF; Couturier J
Cytogenet Cell Genet; 1990; 54(1-2):38-42. PubMed ID: 2249473
[TBL] [Abstract][Full Text] [Related]
22. Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region.
Ogata T; Goodfellow P; Petit C; Aya M; Matsuo N
J Med Genet; 1992 Jul; 29(7):455-9. PubMed ID: 1640423
[TBL] [Abstract][Full Text] [Related]
23. SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite.
Margarit E; Coll MD; Oliva R; Gómez D; Soler A; Ballesta F
Am J Med Genet; 2000 Jan; 90(1):25-8. PubMed ID: 10602113
[TBL] [Abstract][Full Text] [Related]
24. A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies.
Bernstein R; Rosendorff J; Ramsay M; Pinto MR; Page DC
Am J Hum Genet; 1987 Aug; 41(2):145-56. PubMed ID: 3039838
[TBL] [Abstract][Full Text] [Related]
25. Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq.
Bardoni B; Floridia G; Guioli S; Peverali G; Anichini C; Cisternino M; Casalone R; Danesino C; Fraccaro M; Zuffardi O
Hum Genet; 1993 May; 91(4):333-8. PubMed ID: 8099057
[TBL] [Abstract][Full Text] [Related]
26. Sex reversal in a child with duplication of sex reversing locus on the short arm of the X chromosome (Xp).
Ito T; Kaino Y; Hirai H; Kida K; Nakahori Y; Nakagome Y
J Pediatr Endocrinol Metab; 1996; 9(3):429-33. PubMed ID: 8887155
[TBL] [Abstract][Full Text] [Related]
27. X-Y translocations and sex differentiation.
McElreavey K; Cortes LS
Semin Reprod Med; 2001 Jun; 19(2):133-9. PubMed ID: 11480910
[TBL] [Abstract][Full Text] [Related]
28. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
Hsu LY
Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
[TBL] [Abstract][Full Text] [Related]
29. Sex vesicle "entrapment": translocation or nonhomologous recombination of misaligned Yp and Xp as alternative mechanisms for abnormal inheritance of the sex-determining region.
Stalvey JR; Durbin EJ; Erickson RP
Am J Med Genet; 1989 Apr; 32(4):564-72. PubMed ID: 2774010
[TBL] [Abstract][Full Text] [Related]
30. Sex reversal due to Xp disomy by t(X;Y)(p21;q11).
Vasquez AI; Rivera H; Mayorquin A; Mejia-Baltodano G; Escalante A; Sanchez-Corona J
Genet Couns; 1999; 10(3):301-4. PubMed ID: 10546103
[TBL] [Abstract][Full Text] [Related]
31. Molecular investigation of two male subjects with short stature and a 45,X/46,X,ring(Y) karyotype.
Sher ES; Addelston MB; Plotnick L; Urban MD; Berkovitz GD
Horm Res; 1998; 49(1):46-50. PubMed ID: 9438785
[TBL] [Abstract][Full Text] [Related]
32. Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation.
Toublanc JE; Boucekkine C; Abbas N; Barama D; Vilain E; McElreavey K; Toublanc M; Fellous M
Eur J Pediatr; 1993; 152 Suppl 2():S70-5. PubMed ID: 8339747
[TBL] [Abstract][Full Text] [Related]
33. Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height.
Spranger S; Kirsch S; Mertz A; Schiebel K; Tariverdian G; Rappold GA
Clin Genet; 1997 May; 51(5):346-50. PubMed ID: 9212185
[TBL] [Abstract][Full Text] [Related]
34. Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.
Margarit E; Soler A; Carrió A; Oliva R; Costa D; Vendrell T; Rosell J; Ballesta F
J Med Genet; 1998 Sep; 35(9):727-30. PubMed ID: 9733030
[TBL] [Abstract][Full Text] [Related]
35. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter-->q11::q11-->pter).
Fernandez R; Marchal JA; Sanchez A; Pasaro E
Hum Genet; 2002 Sep; 111(3):242-6. PubMed ID: 12215836
[TBL] [Abstract][Full Text] [Related]
36. Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal.
Genuardi M; Bardoni B; Floridia G; Chiurazzi P; Scarano G; Zollino M; Garcea N; Martini-Neri ME; Neri G
Clin Genet; 1995 Jan; 47(1):38-41. PubMed ID: 7774042
[TBL] [Abstract][Full Text] [Related]
37. Cytologic evidence for three human X-chromosomal segments escaping inactivation.
Schempp W; Meer B
Hum Genet; 1983; 63(2):171-4. PubMed ID: 6682404
[TBL] [Abstract][Full Text] [Related]
38. Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion.
Queralt R; Madrigal I; Vallecillos MA; Morales C; Ballescá JL; Oliva R; Soler A; Sánchez A; Margarit E
Am J Med Genet A; 2008 May; 146A(10):1335-40. PubMed ID: 18412126
[TBL] [Abstract][Full Text] [Related]
39. Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.
Joseph M; Cantú ES; Pai GS; Willi SM; Papenhausen PR; Weiss L
J Med Genet; 1996 Nov; 33(11):906-11. PubMed ID: 8950669
[TBL] [Abstract][Full Text] [Related]
40. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.
Kusz K; Kotecki M; Wojda A; Szarras-Czapnik M; Latos-Bielenska A; Warenik-Szymankiewicz A; Ruszczynska-Wolska A; Jaruzelska J
J Med Genet; 1999 Jun; 36(6):452-6. PubMed ID: 10874632
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]