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Results: 1 to 20 of 140

1.

46,XX Testicular Disorder of Sex Development.

Vilain EJ.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2003 Oct 30 [updated 2009 May 26].

PMID:
20301589
[PubMed]
Books & Documents
2.

Two males with SRY-positive 46,XX testicular disorder of sex development.

Gunes S, Asci R, Okten G, Atac F, Onat OE, Ogur G, Aydin O, Ozcelik T, Bagci H.

Syst Biol Reprod Med. 2013 Feb;59(1):42-7. doi: 10.3109/19396368.2012.731624. Epub 2012 Oct 30.

PMID:
23110663
[PubMed - indexed for MEDLINE]
3.

A Korean boy with 46,XX testicular disorder of sex development caused by SOX9 duplication.

Lee GM, Ko JM, Shin CH, Yang SW.

Ann Pediatr Endocrinol Metab. 2014 Jun;19(2):108-12. doi: 10.6065/apem.2014.19.2.108. Epub 2014 Jun 30.

PMID:
25077096
[PubMed]
Free PMC Article
4.

Androgen Insensitivity Syndrome.

Gottlieb B, Beitel LK, Trifiro MA.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
1999 Mar 24 [updated 2014 Jul 10].

PMID:
20301602
[PubMed]
Books & Documents
5.

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive.

Wu QY, Li N, Li WW, Li TF, Zhang C, Cui YX, Xia XY, Zhai JS.

BMC Urol. 2014 Aug 28;14(1):70. doi: 10.1186/1471-2490-14-70.

PMID:
25169080
[PubMed - in process]
Free PMC Article
6.

Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus.

Temel SG, Gulten T, Yakut T, Saglam H, Kilic N, Bausch E, Jin WJ, Leipoldt M, Scherer G.

Sex Dev. 2007;1(1):24-34. doi: 10.1159/000096236.

PMID:
18391513
[PubMed - indexed for MEDLINE]
7.

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]
8.

XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.

Maciel-Guerra AT, de Mello MP, Coeli FB, Ribeiro ML, Miranda ML, Marques-de-Faria AP, Baptista MT, Moraes SG, Guerra-Júnior G.

J Clin Endocrinol Metab. 2008 Feb;93(2):339-43. Epub 2007 Dec 4.

PMID:
18056774
[PubMed - indexed for MEDLINE]
9.

Cytogenic and molecular analyses of 46,XX male syndrome with clinical comparison to other groups with testicular azoospermia of genetic origin.

Chiang HS, Wu YN, Wu CC, Hwang JL.

J Formos Med Assoc. 2013 Feb;112(2):72-8. doi: 10.1016/j.jfma.2012.02.009. Epub 2012 Aug 30.

PMID:
23380608
[PubMed - indexed for MEDLINE]
10.

46,XX male - testicular disorder of sexual differentiation (DSD): hormonal, molecular and cytogenetic studies.

Alves C, Braid Z, Coeli FB, Mello MP.

Arq Bras Endocrinol Metabol. 2010 Nov;54(8):685-9.

PMID:
21340153
[PubMed - indexed for MEDLINE]
Free Article
11.

46,XX male disorder of sexual development:a case report.

Anık A, Çatlı G, Abacı A, Böber E.

J Clin Res Pediatr Endocrinol. 2013;5(4):258-60. doi: 10.4274/Jcrpe.1098.

PMID:
24379036
[PubMed - in process]
Free PMC Article
12.

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]
13.

46,XY Disorder of Sex Development and 46,XY Complete Gonadal Dysgenesis.

Ostrer H.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2008 May 21 [updated 2009 Sep 15].

PMID:
20301714
[PubMed]
Books & Documents
14.
15.

Disorders of sexual development and associated changes in the pituitary-gonadal axis in dogs.

Buijtels JJ, de Gier J, Kooistra HS, Grinwis GC, Naan EC, Zijlstra C, Okkens AC.

Theriogenology. 2012 Oct 15;78(7):1618-26. doi: 10.1016/j.theriogenology.2012.07.010.

PMID:
22980090
[PubMed - indexed for MEDLINE]
16.

A Lack of Association between Polymorphisms of Three Positional Candidate Genes (CLASP2 , UBP1, and FBXL2) and Canine Disorder of Sexual Development (78,XX; SRY -Negative).

Salamon S, Nowacka-Woszuk J, Szczerbal I, Dzimira S, Nizanski W, Ochota M, Switonski M.

Sex Dev. 2014;8(4):160-5. doi: 10.1159/000363531. Epub 2014 Jun 28.

PMID:
24994500
[PubMed - in process]
17.

X-Linked Adrenal Hypoplasia Congenita.

Achermann JC, Vilain EJ.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2001 Nov 20 [updated 2013 Oct 17].

PMID:
20301604
[PubMed]
Books & Documents
18.

Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports.

Gao X, Chen G, Huang J, Bai Q, Zhao N, Shao M, Jiao L, Wei Y, Chang L, Li D, Yang L.

J Assist Reprod Genet. 2013 Mar;30(3):431-5. doi: 10.1007/s10815-013-9939-7. Epub 2013 Feb 3.

PMID:
23378127
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature.

Ergun-Longmire B, Vinci G, Alonso L, Matthew S, Tansil S, Lin-Su K, McElreavey K, New MI.

J Pediatr Endocrinol Metab. 2005 Aug;18(8):739-48.

PMID:
16200839
[PubMed - indexed for MEDLINE]
20.

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]

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