Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 314

1.

An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family.

Slaney SF, Chalmers IJ, Affara NA, Chitty LS.

J Med Genet. 1998 Jan;35(1):17-22. Review.

2.

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 Jr, Duarte MH, Araújo AG, Martelli L.

Hum Genet. 1996 May;97(5):596-8.

PMID:
8655137
3.

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.

4.

Abnormalities of gonadal differentiation.

Berkovitz GD, Seeherunvong T.

Baillieres Clin Endocrinol Metab. 1998 Apr;12(1):133-42. Review.

PMID:
9890065
5.

Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal.

Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC.

Nat Genet. 1996 Oct;14(2):206-9.

PMID:
8841197
6.

Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.

Torres L, López M, Méndez JP, Canto P, Cervantes A, Alfaro G, Pérez-Palacios G, Erickson RP, Kofman-Alfaro S.

Am J Med Genet. 1996 May 17;63(2):348-55.

PMID:
8725784
7.

Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.

Domenice S, Nishi MY, Billerbeck AE, Carvalho FM, Frade EM, Latronico AC, Arnhold IJ, Mendonca BB.

Med Sci Monit. 2001 Mar-Apr;7(2):238-41.

PMID:
11257728
8.

Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.

Lim HN, Berkovitz GD, Hughes IA, Hawkins JR.

Hum Genet. 2000 Dec;107(6):650-2. Epub 2000 Nov 14. Erratum in: Hum Genet. 2004 Aug;115(3):263.

PMID:
11153920
9.

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.

PMID:
9719302
10.

Candidate genes in complete and partial XY sex reversal: mutation analysis of SRY, SRY-related genes and FTZ-F1.

Lim HN, Freestone SH, Romero D, Kwok C, Hughes IA, Hawkins JR.

Mol Cell Endocrinol. 1998 May 25;140(1-2):51-8. Review.

PMID:
9722168
11.

Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis.

Grigorescu-Sido A, Heinrich U, Grigorescu-Sido P, Jauch A, Hager HD, Vogt PH, Duncea I, Bettendorf M.

J Pediatr Endocrinol Metab. 2005 Feb;18(2):197-203.

PMID:
15751609
12.

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 1;322(1208):133-44.

PMID:
2907797
13.

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8590-4.

14.

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, et al.

Clin Endocrinol (Oxf). 1994 Jun;40(6):733-42.

PMID:
8033363
15.

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.

PMID:
8402263
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, et al.

Hum Genet. 1992 Sep-Oct;90(1-2):121-5.

PMID:
1427767
17.

Two SRY-negative XX male brothers without genital ambiguity.

Zenteno JC, López M, Vera C, Méndez JP, Kofman-Alfaro S.

Hum Genet. 1997 Oct;100(5-6):606-10.

PMID:
9341880
18.

Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.

Turner B, Fechner PY, Fuqua JS, Marcantonio SM, Perlman EJ, Vordermark JS, Berkovitz GD.

Am J Med Genet. 1995 Jul 3;57(3):440-3.

PMID:
7677147
19.

A single genetic determinant that prevents sex reversal in C57BL-YPOS congenic mice.

Whitney JB, Mills TM, Lewis RW, Wartell R, Abney TO.

Biochem Genet. 2000 Jun;38(5-6):119-37.

PMID:
11091903
20.

The etiology of XX sex reversal.

de la Chapelle A, Hästbacka J, Korhonen T, Mäenpää J.

Reprod Nutr Dev. 1990;Suppl 1:39s-49s. Review.

PMID:
1976312

Supplemental Content

Support Center