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1دورية أكاديمية
المؤلفون: Maria Tereza Martins Ferrari, Elinaelma Suelane do Nascimento Silva, Mirian Yumie Nishi, Rafael Loch Batista, Berenice Bilharinho Mendonca, Sorahia Domenice
المصدر: Frontiers in Endocrinology, Vol 15 (2024)
مصطلحات موضوعية: differences of sex development (DSD), 46, XX testicular DSD, XX ovotesticular DSD, gonadal development, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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2دورية أكاديمية
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3دورية أكاديمية
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المؤلفون: Hisamitsu Ide, Shinichi Ban, Toshiyuki Iwahata, Akiyoshi Osaka, Hiroshi Okada, Kazutaka Saito, Yoshitomo Kobori, Kentaro Matsuoka
المصدر: American Journal of Men's Health
American Journal of Men's Health, Vol 14 (2020)مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pathology, medicine.medical_specialty, endocrine system, Health (social science), Testicular Disorder, Biopsy, lcsh:Medicine, Case Report, Y chromosome, Male infertility, 03 medical and health sciences, 0302 clinical medicine, Testicular Neoplasms, 030225 pediatrics, SRY, Testis, medicine, Humans, Infertility, Male, Incidental Findings, XX testicular DSD, Chromosomes, Human, Y, medicine.diagnostic_test, business.industry, urogenital system, Sexual Development, lcsh:R, Public Health, Environmental and Occupational Health, Karyotype, medicine.disease, Leydig cell tumor, Sex-Determining Region Y Protein, 030104 developmental biology, Testis determining factor, Leydig Cell Tumor, Female, business, Benign Leydig Cell Tumor, Orchiectomy
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المؤلفون: Frédérique Dijoud, Anne C Tabet, S. Belloc, Sandra Chantot-Bastaraud, Isabelle Goubin-Versini, Caroline Storey, Agathe Hercent, Xavier Ferraretto, Matthieu Peycelon, Jean-François Hermieu, Alexander Valent, Hélène Morel, Edouard Amar, Jean-Pierre Siffroi, Régine Battin-Bertho
المساهمون: Couvet, Sandrine, Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), UF de Génétique moléculaire [CHU Trousseau], CHU Trousseau [APHP], Cabinet d'Andrologie Victor Hugo [Paris], Cerballiance, AP-HP - Hôpital Bichat - Claude Bernard [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Hôpital Robert Debré, Hôpital Robert Debré-Centre Hospitalier Universitaire de Reims (CHU Reims), CH René Dubos, Hospices Civils de Lyon (HCL), Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), UF de Génétique chromosomique [CHU Trousseau], Maladies génétiques d'expression pédiatrique (U933), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
المصدر: Sexual Development
Sexual Development, 2020, 13 (5-6), pp.271-277. ⟨10.1159/000510532⟩مصطلحات موضوعية: Embryology, Gonad, Zygote, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], Embryo, Ovary, Biology, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, medicine.disease, Phenotype, MESH: Human chimeras, Male infertility, Ovotestis, Sex development, XX testicular DSD, Andrology, [SDV] Life Sciences [q-bio], medicine.anatomical_structure, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, medicine, 46, XX/46,XY, Sex organ, Developmental Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0213a4c3587dace1ba9e88bb23aceb36
https://doi.org/10.1159/000510532 -
6دورية أكاديمية
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7دورية أكاديمية
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المؤلفون: Jin, Woo Jung, Leipoldt, Michael, Bausch, Elke, Scherer, Gerd
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Genetik ve Moleküler Biyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı., Temel, Şehime Gülsün, Gülten, Tuna, Yakut, Tahsin, Sağlam, Halil, Kılıç, Neslihan
مصطلحات موضوعية: Male, Chromosome duplication, True Hermaphrodites, Gene loss, 46, Xx Males, Transcription factor Sox9, Embryo development, Gene, Gene locus, Karyotype 46, XX, Mice, Consanguinity, Sex transformation, Testis, Haplotype, 46, XX testicular DSD, Testis disease, Child, Reverse transcriptase polymerase chain reaction, Priority journal, Gene expression regulation, Fluorescence in situ hybridization, Cytogenetic analysis, Sex reversal, Pedigree, Microtubule-associated proteins, Polymerase chain reaction, Sex reversal, gonadal, Phenotype, Female, High mobility group proteins, SOX9, Human, Adult, Adolescent, Child, preschool, Clinical article, Developmental disorder, 46, XX ovotesticular DSD, Sex differentiation, Article, Blood analysis, Deletion, Sex-determining region Y protein, SRY, Campomelic dysplasia, Developmental biology, Transcription factors, Transmission, Humans, Family, Gene mutation, Human tissue, SRY gene, Y chromosome, Neuropeptides, Sex determination, Mutational analysis, Hormones, Sexual development, Testis development, Haplotypes, Mutation, Gonads, Disorders of Sex Development, Sex Determination
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______9458::81e2882883b0934a53c83bbbcbad50ec
http://hdl.handle.net/11452/28649 -
9دورية أكاديمية
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10دورية أكاديمية
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