المؤلفون: Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendeliler

المصدر: JCRPE, Vol 14, Iss 2, Pp 153-171 (2022)

مصطلحات موضوعية: 46, xy disorders of sex development, 5α, -reductase deficiency, androgen insensitivity syndrome, androgen receptor gene mutations, srd5a2 gene mutations, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://jcrpe.org/jvi.aspx?pdir=jcrpe&plng=eng&un=JCRPE-83702&look4=; https://doaj.org/toc/1308-5727; https://doaj.org/toc/1308-5735

URL الوصول: https://doaj.org/article/860a70dc14c9409aacfb6b3de305c261

المؤلفون: Maria Sol Touzon, Natalia Perez Garrido, Roxana Marino, Pablo Ramirez, Mariana Costanzo, Gabriela Guercio, Esperanza Berensztein, Marco A. Rivarola, Alicia Belgorosky

المصدر: JCRPE, Vol 11, Iss 1, Pp 24-33 (2019)

مصطلحات موضوعية: 46, XY disorders of sex development, androgen insensitivity syndrome, androgen receptor gene mutations, mosaicism, clinical phenotype, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: http://www.jcrpe.org/archives/archive-detail/article-preview/androgen-nsensitivity-syndrome-clinical-phenotype-/19687; https://doaj.org/toc/1308-5727; https://doaj.org/toc/1308-5735

URL الوصول: https://doaj.org/article/c6602376e5884b39b76c135a2b3fd8fe

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المؤلفون: Gabriela Guercio, Mariana Costanzo, Alicia Belgorosky, Pablo Ramírez, Natalia Perez Garrido, Esperanza Berensztein, M A Rivarola, Maria Sol Touzon, Roxana Marino

المصدر: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 11, Iss 1, Pp 24-33 (2019)

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Endocrinology, Diabetes and Metabolism, 030105 genetics & heredity, medicine.disease_cause, lcsh:Diseases of the endocrine glands. Clinical endocrinology, Cohort Studies, Tertiary Care Centers, 0302 clinical medicine, Endocrinology, Child, Mutation, education.field_of_study, Mosaicism, lcsh:RJ1-570, purl.org/becyt/ford/3.1 [https], Bioquímica y Biología Molecular, Androgen-Insensitivity Syndrome, Phenotype, Pedigree, Medicina Básica, Receptors, Androgen, Child, Preschool, Female, Original Article, Androgen insensitivity syndrome, purl.org/becyt/ford/3 [https], medicine.medical_specialty, CIENCIAS MÉDICAS Y DE LA SALUD, XY disorders of sex development, Adolescent, medicine.drug_class, Genetic counseling, androgen receptor gene mutations, Population, MOSAICISM, 03 medical and health sciences, Internal medicine, androgen insensitivity syndrome, medicine, Humans, education, Gene, lcsh:RC648-665, Sexual differentiation, business.industry, CLINICAL PHENOTYPE, Infant, Newborn, Infant, lcsh:Pediatrics, Sequence Analysis, DNA, clinical phenotype, Androgen, medicine.disease, Pediatrics, Perinatology and Child Health, XY DISORDERS OF SEX DEVELOPMENT, ANDROGEN RECEPTOR GENE MUTATIONS, business, 030217 neurology & neurosurgery, ANDROGEN INSENSITIVITY SÍNDROME

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40334daebae1efdc17af920dcfc8c508
http://cms.galenos.com.tr/Uploads/Article_19687/JCRPE-0-0-En.pdf

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تسجيل الدخول للوصول الكامل.

المصدر: Journal Of Clinical Research in Pediatric Endocrinology

مصطلحات الفهرس: Endocrinology and metabolism; Pediatrics, 46 XY disorders of sex development; 5a-reductase deficiency; Androgen insensitivity syndrome; Androgen receptor gene mutations; SRD5A2 gene mutations, Journal Article, text/academic publication

URL: http://libdigitalcollections.ku.edu.tr/cdm/ref/collection/IR/id/10402
http://worldcat.org/oclc/1360593545/viewonline
Publisher version
Koç University Institutional Repository