Your search returned 479 results.

Results
	301.	Disorders of sexual development: an overview of 18 years experience in the pediatric Endocrinology Department of Ankara University. [electronic resource] by Ocal, G Berberoğlu, M Siklar, Z Bilir, P Uslu, R Yağmurlu, A Tükün, A Akar, N Soygür, T Gültan, S Gedik, V Tonyukuk Producer: 20110217 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)
	302.	Try235Phe homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Turkish patient. [electronic resource] by Parlak, Mesut Durmaz, Erdem Gursoy, Semin Bircan, Iffet Akcurin, Sema Producer: 20150608 In: Annals of Saudi medicine vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	303.	[MALE PSEUDOHERMAPHRODITISM WITH XY KARYOTYPE AND FEMALE MORPHOLOGY. MULTIPLE GENITAL ANOMALIES. SURGICAL CORRECTION]. [electronic resource] by MUSSET, R BELAISCH, J LAMY, M DE GROUCHY, J NEZELOFF, C Producer: 19961201 In: Gynecologie et obstetrique vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	304.	Longitudinal hormonal evaluation in a patient with disorder of sexual development, 46,XY karyotype and one NR5A1 mutation. [electronic resource] by Pedace, Lucia Laino, Luigi Preziosi, Nicoletta Valentini, Maria Stella Scommegna, Salvatore Rapone, Anna Maria Guarino, Nino Boscherini, Brunetto De Bernardo, Carmelilia Marrocco, Giacinto Majore, Silvia Grammatico, Paola Producer: 20160516 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	305.	Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome. [electronic resource] by Mazen, Inas El-Gammal, Mona McElreavey, Ken Elaidy, Aya Abdel-Hamid, Mohamed S Producer: 20171121 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	306.	Pregnancy and Live Birth In Women With Pathogenic LHCGR Variants Using Their Own Oocytes. [electronic resource] by Lu, Xuefeng Yan, Zheng Cai, Renfei Khor, Shuzin Wu, Ling Sun, Lihua Wang, Yun Xu, Yao Tian, Hui Chen, Qiuju Qiao, Jie Li, Bing Chen, Biaobang Cao, Yu Lyu, Qifeng Wang, Lei Kuang, Yanping Producer: 20200604 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	307.	A novel NR5A1 variant in an infant with elevated testosterone from an Australasian cohort of 46,XY patients with disorders of sex development. [electronic resource] by Wu, Joyce Y McGown, Ivan N Lin, Lin Achermann, John C Harris, Mark Cowley, David M Aftimos, Salim Neville, Kristen A Choong, Catherine S Cotterill, Andrew M Producer: 20130912 In: Clinical endocrinology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	308.	[Questions and dilemmas in the management of hypospadias]. [electronic resource] by Ságodi, László Kiss, Ákos Kiss-Tóth, Emőke Barkai, László Producer: 20141010 In: Orvosi hetilap vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	309.	Adrenarche unmasks compound heterozygous 3β-hydroxysteroid dehydrogenase deficiency: c.244G>A (p.Ala82Thr) and the novel 931C>T (p.Gln311*) variant in a non-salt wasting, severely undervirilised 46XY. [electronic resource] by Teasdale, Stephanie Louise Morton, Adam Producer: 20170822 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	310.	Clinical and molecular characterization of 5α-reductase type 2 deficiency due to mutations (p.Q6X, p.R246Q) in SRD5A2 gene. [electronic resource] by Jia, Wenyu Zheng, Dongmei Zhang, Liya Li, Changzhong Zhang, Xu Wang, Fei Guan, Qingbo Fang, Li Zhao, Jiajun Xu, Chao Producer: 20181024 In: Endocrine journal vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	311.	Growth Hormone Deficiency Causing Micropenis: Lessons Learned From a Well-Adjusted Adult. [electronic resource] by Lee, Peter A Mazur, Tom Houk, Christopher P Blizzard, Robert M Producer: 20190429 In: Pediatrics vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	312.	Rare missense P450c17 (CYP17A1) mutation in exon 1 as a cause of 46,XY disorder of sexual development: implications of breast tissue 'unresponsiveness' despite adequate estradiol substitution. [electronic resource] by Athanasoulia, A P Auer, M Riepe, F G Stalla, G K Producer: 20140416 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	313.	Pubertal Development and Pregnancy Outcomes in 46,XX Patients With Nonclassic Lipoid Congenital Adrenal Hyperplasia. [electronic resource] by Hatabu, Naomi Amano, Naoko Mori, Jun Hasegawa, Yukihiro Matsuura, Hiroki Sumitomo, Naofumi Nishizawa, Kazumichi Suzuki, Mariko Katakura, Satomi Kanamoto, Naokazu Kamimaki, Tsutomu Ishii, Tomohiro Hasegawa, Tomonobu Producer: 20200227 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	314.	Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination. [electronic resource] by Pearlman, Alexander Loke, Johnny Le Caignec, Cedric White, Stefan Chin, Lisa Friedman, Andrew Warr, Nicholas Willan, John Brauer, David Farmer, Charles Brooks, Eric Oddoux, Carole Riley, Bridget Shajahan, Shahin Camerino, Giovanna Homfray, Tessa Crosby, Andrew H Couper, Jenny David, Albert Greenfield, Andy Sinclair, Andrew Ostrer, Harry Producer: 20110118 In: American journal of human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	315.	Mutation Spectrum of STAR and a Founder Effect of the p.Q258* in Korean Patients with Congenital Lipoid Adrenal Hyperplasia. [electronic resource] by Kang, Eungu Kim, Yoon-Myung Kim, Gu-Hwan Lee, Beom Hee Yoo, Han-Wook Choi, Jin-Ho Producer: 20190104 In: Molecular medicine (Cambridge, Mass.) vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	316.	Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency. [electronic resource] by Ji, Wen Zhang, Lu-Yao Li, Fu-Cheng Wang, Yu He, Wei Yin, Qi-Qi Liao, Zhi-Hong Producer: 20181018 In: Asian journal of andrology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	317.	Late diagnosis of 5alpha steroid-reductase deficiency due to IVS12A>G mutation of the SRD5a2 gene in an adolescent girl presented with primary amenorrhea. [electronic resource] by Skordis, Nicos Shammas, Christos Efstathiou, Elisavet Sertedaki, Amalia Neocleous, Vassos Phylactou, Leonidas Producer: 20120201 In: Hormones (Athens, Greece) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	318.	A novel AMH missense mutation in a patient with persistent Müllerian duct syndrome. [electronic resource] by van der Zwan, Y G Brüggenwirth, H T Drop, S L S Wolffenbuttel, K P Madern, G C Looijenga, L H J Visser, J A Producer: 20130506 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	319.	Health-related quality of life and psychological well-being in adults with differences/disorders of sex development. [electronic resource] by Bennecke, Elena Thyen, Ute Grüters, Annette Lux, Anke Köhler, Birgit Producer: 20171010 In: Clinical endocrinology vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	320.	Tri-allelic expression of HLA gene in 46,XX/46,XY chimerism. [electronic resource] by Yang, John Jeongseok Hwang, Sang-Hyun Ko, Dae-Hyun Seo, Eul-Ju Oh, Heung-Bum Producer: 20190624 In: Transplant immunology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 479 results.