المؤلفون: Hong Ouyang, Bo Chen, Na Wu, Ling Li, Runyu Du, Meichen Qian, Wenshu Yu, Yujing He, Xinyan Liu

المصدر: BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-9 (2021)

مصطلحات موضوعية: Congenital adrenal hypoplasia, Hypogonadotropic hypogonadism, DAX1 gene, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1472-6823

URL الوصول: https://doaj.org/article/7f3f12fef4014f9181fd2b64a513de76

المؤلفون: Ouyang, Hong, Chen, Bo, Wu, Na^{Aff1, Aff3}, Li, Ling, Du, Runyu, Qian, Meichen, Yu, Wenshu, He, Yujing, Liu, Xinyan

المصدر: BMC Endocrine Disorders. 21(1)

المؤلفون: Bertalan, Rita^{Aff1, Aff2}, Bencsik, Zsuzsa^Aff3, Mezei, Piroska^Aff4, Vajda, Zsolt^Aff5, Butz, Henriett^{Aff6, Aff7}, Patócs, Attila^{Aff6, Aff7}

المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 46(4):4599-4604

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Domenice, S., Corrêa, R.V., Costa, E.M.F., Nishi, M.Y., Vilain, E., Arnhold, I.J.P., Mendonca, B.B.

المصدر: Brazilian Journal of Medical and Biological Research. January 2004 37(1)

مصطلحات موضوعية: Sex reversal, SRY gene, DAX1 gene, SF1 gene, WNT4 gene

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2004000100020

المؤلفون: Rojek, Aleksandra^Aff1, Flader, Maciej, Malecka, Elzbieta, Niedziela, Marek^{Aff1, Aff2}

المصدر: Hormones: International Journal of Endocrinology and Metabolism. 13(3):413-419

المؤلفون: Khadilkar, Vaman V., Mangtani, Hari R., Jahagirdar, Rahul R., Khatod, Kavita A., Phadke, Nikhil D., Deepa, Pillay S., Khadilkar, Anuradha V.

المصدر: The Indian Journal of Pediatrics. August 2013 80(8):631-635

المؤلفون: S. Domenice, R.V. Corrêa, E.M.F. Costa, M.Y. Nishi, E. Vilain, I.J.P. Arnhold, B.B. Mendonca

المصدر: Brazilian Journal of Medical and Biological Research, Vol 37, Iss 1, Pp 145-150 (2004)

مصطلحات موضوعية: Sex reversal, SRY gene, DAX1 gene, SF1 gene, WNT4 gene, Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2004000100020; https://doaj.org/toc/0100-879X; https://doaj.org/toc/1414-431X

URL الوصول: https://doaj.org/article/5d7c5a1674624432b2c17debf2fbb0bb

المؤلفون: Yeste, Diego, González-Niño, Cristina, Pérez de Nanclares, Guiomar, Pérez-Nanclares, Gustavo, Audi, Laura, Castaño, Luis, Carrascosa, Antonio

المصدر: European Journal of Pediatrics. January 2009 168(1):65-69

المؤلفون: Meichen Qian, Runyu Du, Na Wu, Yujing He, Bo Chen, Xinyan Liu, Ling Li, Hong OuYang, Wenshu Yu

المصدر: BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Endocrine Disorders

مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Case Report, 030209 endocrinology & metabolism, Congenital adrenal hypoplasia, Disease, Hypogonadotropic hypogonadism, Diseases of the endocrine glands. Clinical endocrinology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Hormone replacement therapy (female-to-male), Diabetes mellitus, medicine, Humans, Congenital adrenal hyperplasia, 030212 general & internal medicine, Genetic testing, medicine.diagnostic_test, Adrenal Hyperplasia, Congenital, business.industry, DAX-1 Orphan Nuclear Receptor, Hypogonadism, Genetic Diseases, X-Linked, General Medicine, RC648-665, medicine.disease, Prognosis, DAX1 gene, Hypoadrenocorticism, Familial, Mutation, Slipped capital femoral epiphysis, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a1c5774262cf7888036577571da9ff
https://pubmed.ncbi.nlm.nih.gov/34130666