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	241.	A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1. [electronic resource] by Rivero-Müller, Adolfo Potorac, Iulia Pintiaux, Axelle Daly, Adrian F Thiry, Albert Rydlewski, Catherine Nisolle, Michelle Parent, Anne-Simone Huhtaniemi, Ilpo Beckers, Albert Producer: 20150706 In: European journal of endocrinology vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	242.	A Child with Ambiguous Genitalia: An Atypical Presentation. [electronic resource] by Sheikh, Waqas Hanif Asif, Naveed Younas, Muhammad Basharat, Nida Producer: 20200103 In: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	243.	[Differences of Sex Development (DSD): Controversies and Challenges]. [electronic resource] by Bessiène, Laura Lombès, Marc Bouvattier, Claire Producer: 20181113 In: Annales d'endocrinologie vol. 79 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	244.	Management of children with disorders of sex development: 20-year experience in southern Thailand. [electronic resource] by Jaruratanasirikul, Somchit Engchaun, Vorapun Producer: 20150112 In: World journal of pediatrics : WJP vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	245.	A novel missense mutation in HSD17B3 gene in a 46, XY adolescent presenting with primary amenorrhea and virilization at puberty. [electronic resource] by Tuhan, Hale Unver Anik, Ahmet Catli, Gonul Ceylaner, Serdar Dundar, Bumin Bober, Ece Abaci, Ayhan Producer: 20150728 In: Clinica chimica acta; international journal of clinical chemistry vol. 438 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	246.	Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Müllerian duct syndrome. [electronic resource] by Morikawa, Shuntaro Moriya, Kimihiko Ishizu, Katsura Tajima, Toshihiro Producer: 20150129 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	247.	Understanding the genetic aetiology in patients with XY DSD. [electronic resource] by Ahmed, S F Bashamboo, A Lucas-Herald, A McElreavey, K Producer: 20131217 In: British medical bulletin vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	248.	Excision of Mullerian duct remnant for persistent Mullerian duct syndrome provides favorable short- and mid-term outcomes. [electronic resource] by Wei, C H Wang, N L Ting, W H Du, Y C Fu, Y W Producer: 20150909 In: Journal of pediatric urology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	249.	Quality of life of patients with 46,XX and 46,XY disorders of sex development. [electronic resource] by Amaral, Rita Cassia Inacio, Marlene Brito, Vinicius N Bachega, Tania A S S Domenice, Sorahia Arnhold, Ivo J P Madureira, Guiomar Gomes, Larissa Costa, Elaine M F Mendonca, Berenice B Producer: 20151117 In: Clinical endocrinology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	250.	Novel homozygous mutation in a colombian patient with persistent müllerian duct syndrome: expanded phenotype. [electronic resource] by Acero, Mary García Moreno, Olga Gutiérrez, Andrés Sánchez, Catalina Cataño, Juan Guillermo Suárez-Obando, Fernando Rojas, Adriana Producer: 20191031 In: International braz j urol : official journal of the Brazilian Society of Urology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	251.	Robotic removal of Müllerian duct remnants in pediatric patients: our experience and a review of the literature. [electronic resource] by Lima, Mario Maffi, Michela Di Salvo, Niel Ruggeri, Giovanni Libri, Michele Gargano, Tommaso Lardy, Hubert Producer: 20181102 In: La Pediatria medica e chirurgica : Medical and surgical pediatrics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	252.	Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. [electronic resource] by Portnoi, Marie-France Dumargne, Marie-Charlotte Rojo, Sandra Witchel, Selma F Duncan, Andrew J Eozenou, Caroline Bignon-Topalovic, Joelle Yatsenko, Svetlana A Rajkovic, Aleksandar Reyes-Mugica, Miguel Almstrup, Kristian Fusee, Leila Srivastava, Yogesh Chantot-Bastaraud, Sandra Hyon, Capucine Louis-Sylvestre, Christine Validire, Pierre de Malleray Pichard, Caroline Ravel, Celia Christin-Maitre, Sophie Brauner, Raja Rossetti, Raffaella Persani, Luca Charreau, Eduardo H Dain, Liliana Chiauzzi, Violeta A Mazen, Inas Rouba, Hassan Schluth-Bolard, Caroline MacGowan, Stuart McLean, W H Irwin Patin, Etienne Rajpert-De Meyts, Ewa Jauch, Ralf Achermann, John C Siffroi, Jean-Pierre McElreavey, Ken Bashamboo, Anu Producer: 20190130 In: Human molecular genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	253.	Polycystic ovaries and adrenal insufficiency in a young pubescent female with lipoid congenital adrenal hyperplasia due to splice mutation of the StAR gene: a case report and review of the literature. [electronic resource] by Jehaimi, Cayce T Araiza, Virginia C Batish, Sat D Brosnan, Patrick G Producer: 20110712 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	254.	Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene. [electronic resource] by Furtado, Larissa V Pysher, Theodore Opitz, John Lamb, Randy Comstock, Jessica Batish, Sat Mauch, Teri Nelson, Raoul Zhou, Holly Producer: 20111024 In: Fetal and pediatric pathology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	255.	Male pseudohermaphroditism with mixed germ cell tumor. [electronic resource] by Zhang, Heng Liu, Li-mei Duan, Guang-jie Yao, Hong Chen, Tu-nan Lu, Gen-sheng Producer: 20110526 In: Pediatric blood & cancer vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	256.	Persistent Müllerian duct syndrome: lessons learned from managing a series of eight patients over a 10-year period and review of literature regarding malignant risk from the Müllerian remnants. [electronic resource] by Farikullah, Jasmin Ehtisham, Sarah Nappo, Simona Patel, Leena Hennayake, Supul Producer: 20130205 In: BJU international vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	257.	A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development. [electronic resource] by White, Stefan Hewitt, Jacqueline Turbitt, Erin van der Zwan, Yvonne Hersmus, Remko Drop, Stenvert Koopman, Peter Harley, Vincent Cools, Martine Looijenga, Leendert Sinclair, Andrew Producer: 20120613 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	258.	A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiency. [electronic resource] by Idkowiak, Jan Randell, Tabitha Dhir, Vivek Patel, Pushpa Shackleton, Cedric H L Taylor, Norman F Krone, Nils Arlt, Wiebke Producer: 20120706 In: The Journal of clinical endocrinology and metabolism vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	259.	A Case of Chromosomal Disorders of Sex Development with Transverse Testicular Ectopia Mimicking Mixed Gonadal Dysgenesis. [electronic resource] by Matsumoto, Fumi Matsui, Futoshi Yazawa, Koji Shimada, Kenji Producer: 20180314 In: Urology vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	260.	Lipoid congenital adrenal hyperplasia due to steroid acute regulatory protein (STAR) variants in Three Chinese patients. [electronic resource] by Chen, Hong Zhang, Qianru Chen, Ruimin Yuan, Xin Lin, Xiangquan Yang, Xiaohong Zhang, Ying Producer: 20201104 In: The Journal of steroid biochemistry and molecular biology vol. 200 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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