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Three out of four : a case discussion on ambiguous genitaliaVAN MIL, Edgar G. A. H; HIORT, Olaf.European journal of endocrinology. 2008, Vol 159, issn 0804-4643, S91-S93, SUP1Conference Paper

Disorders of sexual differentiationWARNE, G. L; ZAJAC, J. D.Endocrinology and metabolism clinics of North America. 1998, Vol 27, Num 4, issn 0889-8529, x,945-967 [24 p.]Article

A case of true hermaphroditism reveals an unusual mechanism of twinningSOUTER, Vivienne L; PARISI, Melissa A; NYHOLT, Dale R et al.Human genetics. 2007, Vol 121, Num 2, pp 179-185, issn 0340-6717, 7 p.Article

Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systemsDIPIETROMARIA, Aurélie; BENAYOUN, Bérénice A; TODESCHINI, Anne-Laure et al.Human molecular genetics (Print). 2009, Vol 18, Num 17, pp 3324-3333, issn 0964-6906, 10 p.Article

Looks can be deceiving. CommentaryMATTHEWS, Kellie S.Obstetrics and gynecology (New York. 1953). 2007, Vol 109, Num 6, issn 0029-7844, 1449, 1462 [2 p.]Article

Swyer syndrome : presentation and outcomesMICHALA, L; GOSWAMI, D; CREIGHTON, S. M et al.BJOG (Oxford. Print). 2008, Vol 115, Num 6, pp 737-741, issn 1470-0328, 5 p.Article

New approaches to the Klinefelter syndromeNIESCHLAG, Eberhard; WERLER, Steffi; WISTUBA, Joachim et al.Annales d'endocrinologie. 2014, Vol 75, Num 2, pp 88-97, issn 0003-4266, 10 p.Conference Paper

Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological rolesL'HOTE, David; GEORGES, Adrien; TODESCHIN, Anne Laure et al.Human molecular genetics (Print). 2012, Vol 21, Num 14, pp 3264-3274, issn 0964-6906, 11 p.Article

Ascending aortic aneurysm in a patient with mixed gonadal dysgenesisBAKOTO, N; CORMAN, V; LEGROS, J. J et al.Annales d'endocrinologie. 2011, Vol 72, Num 1, pp 45-47, issn 0003-4266, 3 p.Article

Neuralgic Amyotrophy: Parsonage-Turner SyndromeSTUTZ, Christopher M.The Journal of hand surgery (St. Louis, Mo.). 2010, Vol 35A, Num 12, pp 2104-2106, issn 0363-5023, 3 p.Article

Pure ovarian choriocarinoma mimicking ectopic pregnancy in true hermaphroditismDANQING WANG; YAYI HU; YING HE et al.Acta obstetricia et gynecologica scandinavica. 2009, Vol 88, Num 7, pp 850-852, issn 0001-6349, 3 p.Article

Surgical Treatment of Hermaphroditism: Experience With 25 CasesZHANG JINGDE; XING XIN; GUO ENTAN et al.Annals of plastic surgery. 2009, Vol 63, Num 5, pp 543-551, issn 0148-7043, 9 p.Article

Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian developmentMOUMNE, Lara; DIPIETROMARIA, Aurélie; BATISTA, Frank et al.Human molecular genetics (Print). 2008, Vol 17, Num 7, pp 1010-1019, issn 0964-6906, 10 p.Article

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant allelesBENAYOUN, Bérénice A; CABURET, Sandrine; DIPIETROMARIA, Aurélie et al.Human molecular genetics (Print). 2008, Vol 17, Num 20, pp 3118-3127, issn 0964-6906, 10 p.Article

Turner syndrome and clinical treatmentHJERRILD, Britta E; MORTENSEN, Kristian Havmand; GRAVHOLT, Claus H et al.British medical bulletin. 2008, Vol 86, pp 77-93, issn 0007-1420, 17 p.Article

Bilateral germ cell tumors and androgen insensitivity syndromeSHAHIDI, Homayoon; ROBIA, Mark.Journal of clinical oncology. 2007, Vol 25, Num 29, pp 4686-4688, issn 0732-183X, 3 p.Article

A rare case of ambiguous genitaliaNG, S. F; BOO, N. Y; WU, L. L et al.Singapore medical journal. 2007, Vol 48, Num 9, pp 858-861, issn 0037-5675, 4 p.Article

L'apport de l'imagerie dans le bilan diagnostic chez un nourrisson de 3 mois avec hermaphrodisme vraiHADJIDEKOV, G; KIROVA, G; MINKOV, M et al.Journal de radiologie (Paris). 2007, Vol 88, Num 1, pp 80-83, issn 0221-0363, 4 p., CAH1Article

First Colored Illustration and Detailed Description of Hermaphroditism by a Turkish Surgeon, Serefeddin Sabuncuoglu, in the 15th CenturyDINC, Gulten; YILDIRIM, Ibrahim.Annals of plastic surgery. 2007, Vol 59, Num 6, pp 720-722, issn 0148-7043, 3 p.Article

The laparoscopic management of intersex patients : the preferred approachDENES, Francisco T; COCUZZA, Marcelo A. S; SCHNEIDER-MONTEIRO, Edison D et al.BJU international (Papier). 2005, Vol 95, Num 6, pp 863-867, issn 1464-4096, 5 p.Article

Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregationMOUMNE, Lara; FELLOUS, Marc; VEITIA, Reiner A et al.Human molecular genetics (Print). 2005, Vol 14, Num 23, pp 3557-3564, issn 0964-6906, 8 p.Article

Klinefelter's syndromeLANFRANCO, Fabio; KAMISCHKE, Axel; ZITZMANN, Michael et al.Lancet (British edition). 2004, Vol 364, Num 9430, pp 273-283, issn 0140-6736, 11 p.Article

Ophthalmic features of Turner's syndromeDENNISTON, Ako; BUTLER, L.Eye (London. 1987). 2004, Vol 18, Num 7, pp 680-684, issn 0950-222X, 5 p.Article

Persistent cognitive deficits in adult women with Turner syndromeROSS, J. L; STEFANATOS, G. A; KUSHNER, H et al.Neurology. 2002, Vol 58, Num 2, pp 218-225, issn 0028-3878Article

Syndrome de Turner : Clinique - génétique - thérapeutique : L'hormone de croissance (2éme partie) = Turner syndrome : Clinical aspects -genetic aspects - therapyCABROL, S; BOURCIGAUX, N; GICQUEL, C et al.Revue internationale de pédiatrie. 2000, Num 302, pp 25-32, issn 0048-8135Article

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