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

Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutationsMAIMOUN, L; PHILIBERT, P; CAMMAS, B et al.International journal of andrology (Print). 2010, Vol 33, Num 6, pp 841-847, issn 0105-6263, 7 p.Article

Problématique de la prise en charge des anomalies de la différenciation sexuelle dans le service d'urologie: CHU Point G = Issues inherent to the management of disorders of sex development in point G HospitalDIAKITE, M. L; BERTHE H, J. G; TIMBELY, A et al.Progrès en urologie (Paris). 2013, Vol 23, Num 1, pp 66-72, issn 1166-7087, 7 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

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

Comment orienter la démarche diagnostique devant un hypospadias ? = How hypospadias should be investigated?BOUVATTIER, C; GAY, C.-L; BOUGNERES, P et al.Archives de pédiatrie (Paris). 2009, Vol 16, Num 6, pp 948-950, issn 0929-693X, 3 p.Conference Paper

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

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

Treatment of Turner's syndrome during transitionGAWLIK, Aneta; MALECKA-TENDERA, Ewa.European journal of endocrinology. 2014, Vol 170, Num 2, issn 0804-4643, R57-R74Article

Identification of novel SRY mutations and SFI (NR5AI) changes in patients with pure gonadal dysgenesis and 46,XY karyotypePALIWAL, Preeti; SHARMA, Anshul; BIRLA, Shweta et al.Molecular human reproduction. 2011, Vol 17, Num 5-6, pp 372-378, issn 1360-9947, 7 p.Article

Abnormal streak gonads in 46,XY complete gonadal dysgenesisDOHERTY, Leo F; RACKOW, Beth W.Fertility and sterility. 2011, Vol 96, Num 6, pp 1415-1416, issn 0015-0282, 2 p.Article

13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restrictionANDRESEN, J. H; AFTIMOS, S; DOHERTY, E et al.Acta paediatrica (Oslo). 2010, Vol 99, Num 5, pp 784-786, issn 0803-5253, 3 p.Article

Parsonage-Turner Syndrome in a major burns patientWATTS, Guy; FALDER, Sian; REA, Suzanne et al.Burns. 2009, Vol 35, Num 7, pp 1038-1041, issn 0305-4179, 4 p.Article

Long-Term Outcome of Vaginoplasty With the Bilateral Labioscrotal Flap. CommentaryMORIYA, Kimihiko; HIGASHIYAMA, Hiroshi; TANAKA, Hiroshi et al.The Journal of urology. 2009, Vol 182, Num 4, pp 1876-1881, issn 0022-5347, 6 p., 2Conference Paper

A modified approach for feminizing genitoplastySAVANELLI, A; ALICCHIO, F; ESPOSITO, C et al.World journal of urology (Print). 2008, Vol 26, Num 5, pp 517-520, issn 0724-4983, 4 p.Article

Fatal Lung Fibrosis Associated With Immunodeficiency and Gonadal Dysgenesis in 46XX Sisters : A New SyndromeSOMECH, Raz; SOMERS, Gino R; CHITAYAT, David et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 1, pp 8-14, issn 1552-4825, 7 p.Article

Issues in the Diagnosis and Management of Disorders of Sexual Development : PEDIATRIC ENDOCRINOLOGY-1KHADILKAR, Vaman V; PHANSE-GUPTE, Supriya.Indian journal of pediatrics. 2014, Vol 81, Num 1, pp 66-75, issn 0019-5456, 10 p.Article