215 related articles for article (PubMed ID: 8262517)
1. Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences.
Kuhnle U; Schwarz HP; Löhrs U; Stengel-Ruthkowski S; Cleve H; Braun A
Hum Genet; 1993 Dec; 92(6):571-6. PubMed ID: 8262517
[TBL] [Abstract][Full Text] [Related]
2. Familial 46,XX males coexisting with familial 46,XX true hermaphrodites in same pedigree.
Skordis NA; Stetka DG; MacGillivray MH; Greenfield SP
J Pediatr; 1987 Feb; 110(2):244-8. PubMed ID: 3806296
[TBL] [Abstract][Full Text] [Related]
3. Familial XX chromosomal maleness does not arise from a Y chromosomal translocation.
Ostrer H; Wright G; Clayton M; Skordis N; MacGillivray MH
J Pediatr; 1989 Jun; 114(6):977-82. PubMed ID: 2723912
[TBL] [Abstract][Full Text] [Related]
4. The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism.
Berkovitz GD; Fechner PY; Marcantonio SM; Bland G; Stetten G; Goodfellow PN; Smith KD; Migeon CJ
Hum Genet; 1992 Feb; 88(4):411-6. PubMed ID: 1740318
[TBL] [Abstract][Full Text] [Related]
5. Accidental X-Y recombination and the aetiology of XX males and true hermaphrodites.
Ferguson-Smith MA; Affara NA
Philos Trans R Soc Lond B Biol Sci; 1988 Dec; 322(1208):133-44. PubMed ID: 2907797
[TBL] [Abstract][Full Text] [Related]
6. The Y-chromosomal and autosomal testis-determining genes.
de la Chapelle A
Development; 1987; 101 Suppl():33-8. PubMed ID: 3503720
[TBL] [Abstract][Full Text] [Related]
7. SRY-negative true hermaphrodites and an XX male in two generations of the same family.
Ramos ES; Moreira-Filho CA; Vicente YA; Llorach-Velludo MA; Tucci S; Duarte MH; Araújo AG; Martelli L
Hum Genet; 1996 May; 97(5):596-8. PubMed ID: 8655137
[TBL] [Abstract][Full Text] [Related]
8. Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.
Fechner PY; Rosenberg C; Stetten G; Cargile CB; Pearson PL; Smith KD; Migeon CJ; Berkovitz GD
Cytogenet Cell Genet; 1994; 66(1):22-6. PubMed ID: 8275702
[TBL] [Abstract][Full Text] [Related]
9. Familial disorder of sex determination in seven individuals from three related sibships.
Jarrah N; El-Shanti H; Khier A; Obeidat FN; Haddidi A; Ajlouni K
Eur J Pediatr; 2000 Dec; 159(12):912-8. PubMed ID: 11131351
[TBL] [Abstract][Full Text] [Related]
10. Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome.
Damiani D; Billerbeck AE; Goldberg AC; Setian N; Fellous M; Kalil J
Hum Genet; 1990 Jun; 85(1):85-8. PubMed ID: 2358305
[TBL] [Abstract][Full Text] [Related]
11. Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female.
Pereira ET; de Almeida JC; Gunha AC; Patton M; Taylor R; Jeffery S
J Med Genet; 1991 Sep; 28(9):591-5. PubMed ID: 1956056
[TBL] [Abstract][Full Text] [Related]
12. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.
Boucekkine C; Toublanc JE; Abbas N; Chaabouni S; Ouahid S; Semrouni M; Jaubert F; Toublanc M; McElreavey K; Vilain E
Clin Endocrinol (Oxf); 1994 Jun; 40(6):733-42. PubMed ID: 8033363
[TBL] [Abstract][Full Text] [Related]
13. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.
Abbas N; McElreavey K; Leconiat M; Vilain E; Jaubert F; Berger R; Nihoul-Fekete C; Rappaport R; Fellous M
C R Acad Sci III; 1993; 316(4):375-83. PubMed ID: 8402263
[TBL] [Abstract][Full Text] [Related]
14. XX true hermaphroditism in southern African blacks: exclusion of SRY sequences and uniparental disomy of the X chromosome.
Spurdle AB; Shankman S; Ramsay M
Am J Med Genet; 1995 Jan; 55(1):53-6. PubMed ID: 7702097
[TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular analysis of XX sex reversed patients.
Kolon TF; Ferrer FA; McKenna PH
J Urol; 1998 Sep; 160(3 Pt 2):1169-72; discussion 1178. PubMed ID: 9719302
[TBL] [Abstract][Full Text] [Related]
16. A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY.
McElreavey K; Rappaport R; Vilain E; Abbas N; Richaud F; Lortat-Jacob S; Berger R; Le Coniat M; Boucekkine C; Kucheria K
Hum Genet; 1992; 90(1-2):121-5. PubMed ID: 1427767
[TBL] [Abstract][Full Text] [Related]
17. The etiology of XX sex reversal.
de la Chapelle A; Hästbacka J; Korhonen T; Mäenpää J
Reprod Nutr Dev; 1990; Suppl 1():39s-49s. PubMed ID: 1976312
[TBL] [Abstract][Full Text] [Related]
18. A possible common origin of "Y-negative" human XX males and XX true hermaphrodites.
Abbas NE; Toublanc JE; Boucekkine C; Toublanc M; Affara NA; Job JC; Fellous M
Hum Genet; 1990 Mar; 84(4):356-60. PubMed ID: 2307458
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Molecular analysis of sex determination in sex-reversed and true hermaphroditism.
Copelli SB; Bergadá C; Billerbeck AE; Goldberg AC; Kalil J; Damiani D; Targovnik HM
Braz J Med Biol Res; 1996 Jun; 29(6):743-8. PubMed ID: 9070386
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
