المؤلفون: Lingping Li, Xijing Liu, Qinqin Li, Lili Zhang, Yueyue Xiong, Shanling Liu, He Wang, Hongmei Zhu, Xuemei Zhang

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: chromosome mosaicism, prenatal diagnosis, nuchal cystic hygroma, monosomy X, genetic testing, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1165019/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/0d9189a502324dd69c2a32baaa2b6d75

المؤلفون: Labrosse, Julie^Aff3, Grynberg, Michael^{Aff4, Aff5}

المساهمون: Grynberg, Michael, editor^Aff1, Patrizio, Pasquale, editor^Aff2

المصدر: Female and Male Fertility Preservation. :247-262

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المؤلفون: Soares, Jéssica Silva, Lago, Renata Maria Rabello da Silva, Toralles, Maria Betânia Pereira, Mota, Laís Ribeiro, Alves, Esmeralda Santos, Carvalho, Acácia Fernandes Lacerda de

المصدر: Archives of Endocrinology and Metabolism. December 2021 65(6)

مصطلحات موضوعية: Turner syndrome, PCR, FISH technique, mosaicism, monosomy X

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972021000600739

المؤلفون: Dykgraaf, Ramon^Aff3, van den Hoven, Allard^Aff4, Mijnarends-Akkermans, Helen^Aff5

المساهمون: van Weert, Nico, editor^Aff1, Hazelzet, Jan, editor^Aff2

المصدر: Personalized Specialty Care : Value-Based Healthcare Frontrunners from the Netherlands. :79-86

المؤلفون: Levitsky, Lynne L.^{Aff3, Aff4}

المساهمون: Stanley, Takara, editor^Aff1, Misra, Madhusmita, editor^Aff2

المصدر: Endocrine Conditions in Pediatrics : A Practical Guide. :275-279

المؤلفون: Jéssica Silva Soares, Renata Maria Rabello da Silva Lago, Maria Betânia Pereira Toralles, Laís Ribeiro Mota, Esmeralda Santos Alves, Acácia Fernandes Lacerda de Carvalho

المصدر: Archives of Endocrinology and Metabolism, Vol 65, Iss 6, Pp 739-746 (2021)

مصطلحات موضوعية: Turner syndrome, PCR, FISH technique, mosaicism, monosomy X, Medicine, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972021000600739&tlng=en; https://doaj.org/toc/2359-4292

URL الوصول: https://doaj.org/article/d9ef12af76e8411c8b8b068f12746555

المؤلفون: Roberts, Alissa J.^Aff2, Fechner, Patricia Y.^Aff2

المساهمون: Fechner, Patricia Y., editor^Aff1

المصدر: Turner Syndrome : Pathophysiology, Diagnosis and Treatment. :1-12

المؤلفون: Nunes, Maurício Rouvel, Pereira, Tiago Godói, Correia, Henry Victor Dutra, Canabarro, Simone Travi, Vanz, Ana Paula, Zen, Paulo Ricardo Gazzola, Rosa, Rafael Fabiano Machado

المصدر: Sao Paulo Medical Journal. May 2021 139(5)

مصطلحات موضوعية: Turner syndrome, Genetic diseases, inborn, Karyotype, Diagnostic techniques and procedures, X chromosome, Ullrich-Turner syndrome, Monosomy X, Genetic disorders

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802021000500435

المؤلفون: Maurício Rouvel Nunes, Tiago Godói Pereira, Henry Victor Dutra Correia, Simone Travi Canabarro, Ana Paula Vanz, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa

المصدر: São Paulo Medical Journal, Vol 139, Iss 5, Pp 435-442 (2021)

مصطلحات موضوعية: Turner syndrome, Genetic diseases, inborn, Karyotype, Diagnostic techniques and procedures, X chromosome, Ullrich-Turner syndrome, Monosomy X, Genetic disorders, Medicine

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802021000500435&tlng=en; https://doaj.org/toc/1806-9460

URL الوصول: https://doaj.org/article/769c45560ab14f7f8e33e07a9b8d8524