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	321.	Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea. [electronic resource] by Ben Hadj Hmida, Imen Mougou-Zerelli, Soumaya Hadded, Anis Dimassi, Sarra Kammoun, Molka Bignon-Topalovic, Joelle Bibi, Mohamed Saad, Ali Bashamboo, Anu McElreavey, Ken Producer: 20170713 In: Fertility and sterility vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	322.	Serum steroid profiling in Cushing's syndrome patients. [electronic resource] by Hána, Václav Ježková, Jana Kosák, Mikuláš Kršek, Michal Hána, Václav Hill, Martin Producer: 20200121 In: The Journal of steroid biochemistry and molecular biology vol. 192 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	323.	A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in [electronic resource] by Unal, Edip Yıldırım, Ruken Taş, Funda Feryal Tekin, Suat Ceylaner, Serdar Haspolat, Yusuf Kenan Producer: 20210527 In: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	324.	Review and management of 46,XY disorders of sex development. [electronic resource] by Massanyi, Eric Z Dicarlo, Heather N Migeon, Claude J Gearhart, John P Producer: 20140109 In: Journal of pediatric urology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	325.	P450c17 deficiency caused by compound heterozygosity for two novel mutations presenting as hypotension in early infancy. [electronic resource] by Gregg, Brigid Kociolek, Larry K Qin, Kenan Rosenfield, Robert L Yu, Christine Producer: 20120416 In: Hormone research in paediatrics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	326.	Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study. [electronic resource] by Köhler, Birgit Kleinemeier, Eva Lux, Anke Hiort, Olaf Grüters, Annette Thyen, Ute Producer: 20120409 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)
	327.	Successful testicular sperm recovery and IVF treatment in a man with Leydig cell hypoplasia. [electronic resource] by Bakircioglu, M E Tulay, P Findikli, N Erzik, B Gultomruk, M Bahceci, M Producer: 20150330 In: Journal of assisted reproduction and genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	328.	CANINE HEMOPHILIA AND MALE PSEUDOHERMAPHRODITISM; CYTOGENETIC STUDIES. [electronic resource] by BROWN, R C SWANTON, M C BRINKHOUS, K M Producer: 19961201 In: Laboratory investigation; a journal of technical methods and pathology vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	329.	Androgen insensitivity syndrome in a cohort of Sri Lankan children with 46, XY disorders of sex development (46, XY DSD). [electronic resource] by de Silva, K S H Sirisena, N D Wijenayaka, H K Cooray, J G Jayasekara, R W Dissanayake, V H W Producer: 20161213 In: The Ceylon medical journal vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	330.	5α-Reductase type 2 deficiency in families from an isolated Andean population in Venezuela. [electronic resource] by Avendaño, Andrea González-Coira, Mercedes Paradisi, Irene Rojas, Ascanio Da Silva, Gloria Gómez-Pérez, Roald Ceballos, Jesús Osuna Producer: 20210204 In: Annals of human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	331.	17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up. [electronic resource] by Faienza, M F Baldinotti, F Marrocco, G TyuTyusheva, N Peroni, D Baroncelli, G I Bertelloni, S Producer: 20210827 In: Journal of endocrinological investigation vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	332.	DSD due to 5α-reductase 2 deficiency - from diagnosis to long term outcome. [electronic resource] by Costa, Elaine M F Domenice, Sorahia Sircili, Maria Helena Inacio, Marlene Mendonca, Berenice B Producer: 20130314 In: Seminars in reproductive medicine vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	333.	A missense mutation of the Dhh gene is associated with male pseudohermaphroditic rats showing impaired Leydig cell development. [electronic resource] by Kawai, Yasuhiro Noguchi, Junko Akiyama, Kouyou Takeno, Yuriko Fujiwara, Yasuhiro Kajita, Shimpei Tsuji, Takehito Kikuchi, Kazuhiro Kaneko, Hiroyuki Kunieda, Tetsuo Producer: 20110527 In: Reproduction (Cambridge, England) vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	334.	Novel compound heterozygous variants in the LHCGR gene identified in a subject with Leydig cell hypoplasia type 1. [electronic resource] by Xu, Yufei Chen, Yulin Li, Niu Hu, Xuyun Li, Guoqiang Ding, Yu Li, Juan Shen, Yiping Wang, Xiumin Wang, Jian Producer: 20180905 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	335.	Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene. [electronic resource] by Lekarev, Oksana Mallet, Delphine Yuen, Tony Morel, Yves New, Maria I Producer: 20121016 In: European journal of pediatrics vol. 171 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	336.	[Primary hyperaldosteronism]. [electronic resource] by Lüthi, S Zimmerli, L Suter, P M Battegay, E Producer: 20110418 In: Praxis vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	337.	Macrosomia and ambiguous genitalia: a long overdue answer to the citizens of Frusino. [electronic resource] by Vasileiou, Vasiliki Armeni, Anastasia K Pierris, Apostolos L Georgopoulos, Neoklis A Producer: 20130624 In: Hormones (Athens, Greece) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	338.	Hernia uteri inguinalis in a case of ovotesticular disorder of sexual differentiation. [electronic resource] by Venkataram, Aniketh Shivaswamy, Sadashivaiah Babu, Rajashekara Santhosh, Shivashankar Producer: 20130717 In: Journal of pediatric and adolescent gynecology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	339.	[Clinical features and StAR gene mutations in children with congenital lipoid adrenal hyperplasia]. [electronic resource] by Xie, Ting Zheng, Ji-Peng Huang, Yong-Lan Fan, Chun Wu, Dong-Yan Tan, Min-Yi Li, Xiu-Zhen Cheng, Jing Liu, Li Producer: 20150910 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	340.	Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development. [electronic resource] by Sudhakar, Digumarthi V S Jaishankar, Shveta Regur, Phanindranath Kumar, Umesh Singh, Raghvendra Kabilan, Usha Namduri, Sree Dhyani, Jaishree Gupta, Nalini J Chakravarthy, Baidyanath Vaman, Khadilkar Shabir, Iram Khadgawat, Rajesh Deenadayal, Mamata Chaitanya A, Datar Dada, Rima Sharma, Yogendra Anand, Anuranjan Thangaraj, Kumarasamy Producer: 20200814 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 479 results.