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Items: 1 to 20 of 52

1.

A new variant of human intersex with discussion on the developmental aspects.

SHAH PN, NAIK SN, MAHAJAN DK, DAVE MJ, PAYMASTER JC.

Br Med J. 1961 Aug 19;2(5250):474-7. No abstract available.

2.

Twin brothers with MIDAS syndrome and XX karyotype.

Anguiano A, Yang X, Felix JK, Hoo JJ.

Am J Med Genet A. 2003 May 15;119A(1):47-9.

PMID:
12707958
3.

Steroid sulphatase levels in XX males, including observations on two affected cousins.

Pierella P, Craig I, Bobrow M, de la Chapelle A.

Hum Genet. 1981;59(1):87-8.

PMID:
10819031
4.

An SRY-negative XX male with Huriez syndrome.

Vernole P, Terrinoni A, Didona B, De Laurenzi V, Rossi P, Melino G, Grimaldi P.

Clin Genet. 2000 Jan;57(1):61-6.

PMID:
10733237
5.

Prenatal diagnosis of 46,XY/46,XX mosaicism: a case report.

Yaron Y, Feldman B, Kramer RL, Kasperski SB, Vo T, Feldman GL, Johnson MP, Evans MI, Ebrahim SA.

Am J Med Genet. 1999 May 7;84(1):12-4.

PMID:
10213039
6.

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.

7.

Second 46,XX male with MLS syndrome.

Stratton RF, Walter CA, Paulgar BR, Price ME, Moore CM.

Am J Med Genet. 1998 Feb 26;76(1):37-41.

PMID:
9508062
8.

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
9.

SRY-negative XX fetus with complete male phenotype.

Vilain E, Le Fiblec B, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y, Jaubert F, Boucekkine C, McElreavey K, Vekemans M, et al.

Lancet. 1994 Jan 22;343(8891):240-1. No abstract available.

PMID:
7904700
10.

Detection of 46,XX male by Y-specific whole chromosome paint probe.

Jalal SM, Law ME, Dewald GW, Sekhor GS, Van Dyke DL.

Am J Med Genet. 1994 Aug 15;52(2):239-41. No abstract available.

PMID:
7802019
11.

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
12.

Clinical traits and molecular findings in 46,XX males.

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

Clin Genet. 1995 Jul;48(1):29-34.

PMID:
7586641
13.

The XX male -- report on a child and an adult.

Bauch K, Witkowski R, Ullrich E, Dempe A, Lindner J.

Endokrinologie. 1980 Jul;76(1):63-7.

PMID:
7192212
14.

XX male with breast cancer.

Giammarini A, Rocchi M, Zennaro W, Filippi G.

Clin Genet. 1980 Aug;18(2):103-8.

PMID:
7192192
15.

Steroid sulfatase activity in cultured fibroblasts of XX males.

Ropers HH, Migl B, Zimmer J, Müller CR.

Cytogenet Cell Genet. 1981;30(3):168-73. No abstract available.

16.

Gonadotropin dynamics in XX males.

Pérez-Palacios G, Medina M, Ullao-Aguirre A, Chávez BA, Villareal G, Dutrem MT, Cahill LT, Wachtel S.

J Clin Endocrinol Metab. 1981 Aug;53(2):254-7.

PMID:
6788790
17.

An XX male with a single STS gene dose.

Wieacker P, Voiculescu J, Müller CR, Ropers HH.

Cytogenet Cell Genet. 1983;35(1):72-4.

PMID:
6572129
18.

Body size and shape in 46,XX males: an anthropometric investigation.

Varrela J.

Ann Hum Genet. 1984 Jul;48(Pt 3):261-7.

PMID:
6540543
19.

Paternal transmission of maleness in XX human beings.

Kasdan R, Nankin HR, Troen P, Wald N, Pan S, Yanaihara T.

N Engl J Med. 1973 Mar 15;288(11):539-45. No abstract available.

PMID:
4685451
20.

Letter: Pairing of X and Y chromosomes.

Borgaonkar DS.

Lancet. 1974 Sep 14;2(7881):667. No abstract available.

PMID:
4137796

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