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Results: 1 to 20 of 156

1.

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion.

Tar A, Sólyom J, Györvári B, Ion A, Telvi L, Barbaux S, Souleyreau N, Vilain E, Fellous M, McElreavey K.

Hum Genet. 1995 Oct;96(4):464-8.

PMID:
7557971
[PubMed - indexed for MEDLINE]
2.

Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA.

Jiménez AL, Kofman-Alfaro S, Berumen J, Hernández E, Canto P, Méndez JP, Zenteno JC.

Am J Med Genet. 2000 Aug 28;93(5):417-20.

PMID:
10951467
[PubMed - indexed for MEDLINE]
3.

Detection of the sex-determining region of the Y chromosome in 46,XX true hermaphroditism.

Kojima Y, Hayashi Y, Asai N, Maruyama T, Sasaki S, Kohri K.

Urol Int. 1998 Aug;60(4):235-8.

PMID:
9701737
[PubMed - indexed for MEDLINE]
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.

PMID:
1740318
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditism.

Tanoue A, Nakamura T, Endo F, Nishiyama S, Sakiyama H, Matsuda I.

Jpn J Hum Genet. 1992 Dec;37(4):311-20.

PMID:
1297452
[PubMed - indexed for MEDLINE]
7.
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.

PMID:
8275702
[PubMed - indexed for MEDLINE]
9.

A rare case of 46,XX true hermaphroditism with hidden mosaicism with sex-determining region Y chromosome-bearing cells in the gonads.

Inoue H, Nomura M, Yanase T, Ichino I, Goto K, Ikuyama S, Takayanagi R, Nawata H.

Intern Med. 1998 May;37(5):467-71.

PMID:
9652903
[PubMed - indexed for MEDLINE]
Free Article
10.

Sry-negative XX sex reversal in a family of Norwegian Elkhounds.

Melniczek JR, Dambach D, Prociuk U, Jezyk PF, Henthorn PS, Patterson DF, Giger U.

J Vet Intern Med. 1999 Nov-Dec;13(6):564-9. Review.

PMID:
10587257
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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, et al.

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

PMID:
8033363
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
1956056
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

True hermaphroditism associated with microphthalmia.

Hayashi T, Kageyama Y, Ishizaka K, Tsujii T, Oshima H.

Eur J Endocrinol. 1999 Jan;140(1):62-5.

PMID:
10037254
[PubMed - indexed for MEDLINE]
Free Article
16.

45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism.

Nieto K, Peña R, Palma I, Dorantes LM, Eraña L, Alvarez R, García-Cavazos R, Kofman-Alfaro S, Queipo G.

Am J Med Genet A. 2004 Oct 15;130A(3):311-4.

PMID:
15378545
[PubMed - indexed for MEDLINE]
17.

Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation.

Ogata T, Hawkins JR, Taylor A, Matsuo N, Hata J, Goodfellow PN.

J Med Genet. 1992 Apr;29(4):226-30.

PMID:
1583640
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

True hermaphroditism: genetic variants and clinical management.

Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M, Nihoul-Fékété C, Rappaport R.

J Pediatr. 1994 Nov;125(5 Pt 1):738-44.

PMID:
7965425
[PubMed - indexed for MEDLINE]
19.

[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].

Reichenbach H, Holland H, Thamm B, Theile T.

Kinderarztl Prax. 1993 Oct;61(7-8):291-5. German.

PMID:
8271681
[PubMed - indexed for MEDLINE]
20.

Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3).

Sanlaville D, Vialard F, Thépot F, Vue-Droy L, Ardalan A, Nizard P, Corré A, Devauchelle B, Martin-Denavit T, Nouchy M, Malan V, Taillemite JL, Portnoï MF.

Am J Med Genet A. 2004 Jul 30;128A(3):325-30.

PMID:
15216557
[PubMed - indexed for MEDLINE]

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