المؤلفون: Sang Hoon Yoon, Ga Yeon Kim, Gyu Tae Choi, Jeong Tae Do

المصدر: Cells, Vol 12, Iss 10, p 1365 (2023)

مصطلحات موضوعية: Turner syndrome, X monosomy, X chromosome inactivation, organ abnormalities, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/12/10/1365; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/82d505c922754c0b9ff5bd1c7fb12a5c

المؤلفون: Lynn, Phoebe M. Y., Stergiakouli, Evangelia, Davies, William^Aff1_1

المساهمون: Clelland, James D, editor^AffID1

المصدر: Genomics, Proteomics, and the Nervous System. 2:3-20

المؤلفون: Dionora Araque, Francisco R. Cammarata Scalisi, María Angelina Lacruz Rengel, Fabiola López

المصدر: Avances en Biomedicina, Vol 2, Iss 3, Pp 121-126 (2013)

مصطلحات موضوعية: Alteración cromosómica, trisomía 21, monosomía del X, Chromosomal abnormality, trisomy 21 X monosomy, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://erevistas.saber.ula.ve/index.php/biomedicina/article/view/4448; https://doaj.org/toc/2244-7881

URL الوصول: https://doaj.org/article/57ac653f8c554261884ee45c3c84a99e

المؤلفون: Silva, Aline Lourenço da, Lima, Renata LL Ferreira de, Ribeiro, Lucilene Arilho, Moretti-Ferreira, Danilo

المصدر: Genetics and Molecular Biology. January 2006 29(1)

مصطلحات موضوعية: Robertsonian translocation, X monosomy, interchromosomal effect

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100010

المؤلفون: N Bourcigaux, A. Khodawardi, Jean-Pierre Siffroi, A. Graff, Sophie Christin-Maitre, Camille Vatier, M.C. Villy, A. Borgel, B. Donadille, H. Morel

المساهمون: Sorbonne Université (SU), Service d'Endocrinologie, diabétologie et endocrinologie de la reproduction [CHU Saint-Antoine], CHU Saint-Antoine [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), UF de Génétique chromosomique [CHU Trousseau], Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], Couvet, Sandrine

المصدر: Human Reproduction
Human Reproduction, 2020, 35 (10), pp.2391-2398. ⟨10.1093/humrep/deaa197⟩

مصطلحات موضوعية: MESH: Mouth Mucosa, [SDV]Life Sciences [q-bio], Buccal swab, blood karyotype, Turner Syndrome, [SDV.GEN] Life Sciences [q-bio]/Genetics, Cohort Studies, 0302 clinical medicine, Turner syndrome, Medicine, X/46, Prospective Studies, MESH: Cohort Studies, Ovarian Neoplasms, 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, Mosaicism, Rehabilitation, Obstetrics and Gynecology, [SDV] Life Sciences [q-bio], MESH: Ovarian Neoplasms, buccal cells FISH, Cohort, Female, MESH: Mosaicism, Cohort study, Adult, medicine.medical_specialty, MESH: Turner Syndrome, Urinary system, Gonadoblastoma, 030209 endocrinology & metabolism, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, 03 medical and health sciences, Internal medicine, Humans, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, business.industry, Mouth Mucosa, Turner’s syndrome, MESH: Adult, Buccal administration, medicine.disease, MESH: Prospective Studies, Reproductive Medicine, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Skin biopsy, business, MESH: Female, X monosomy, XX mosaicism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb39d17380e1193e2a9d1a0edfd5372
https://www.hal.inserm.fr/inserm-03857359

المؤلفون: Bondy, Carolyn A., Cheng, Clara

المصدر: Chromosome Research: Cytogenetics, genomics, chromatin and the nucleus. July 2009 17(5):649-658

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المؤلفون: Aline Lourenço da Silva, Renata LL Ferreira de Lima, Lucilene Arilho Ribeiro, Danilo Moretti-Ferreira

المصدر: Genetics and Molecular Biology, Vol 29, Iss 1, Pp 47-48 (2006)

مصطلحات موضوعية: Robertsonian translocation, X monosomy, interchromosomal effect, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100010; https://doaj.org/toc/1415-4757; https://doaj.org/toc/1678-4685

URL الوصول: https://doaj.org/article/8073bd32f246468eacd10169987bc073

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