المؤلفون: Mačkić-Đurović, Mirela¹ mirelamd@yahoo.com, Stomornjak-Vukadin, Meliha², Ibrulj, Slavka¹

المصدر: Iranian Journal of Medical Sciences. Jul2018, Vol. 43 Issue 4, p436-439. 4p.

مصطلحات موضوعية: *DIAGNOSIS of Down syndrome, *TURNER'S syndrome, *CHROMOSOME banding, *GENETIC counseling, *INFERTILITY, *KARYOTYPES, *MOSAICISM, *FLUORESCENCE in situ hybridization, *FLUORESCENT dyes, *GENETICS, *DIAGNOSIS

المؤلفون: Bucerzan, Simona¹, Miclea, Diana^1,2 bolca12diana@yahoo.com, Popp, Radu², Alkhzouz, Camelia¹, Lazea, Cecilia¹, Pop, Ioan Victor², Grigorescu-Sido, Paula¹

المصدر: Therapeutics & Clinical Risk Management. May2017, Vol. 13, p613-622. 10p.

مصطلحات موضوعية: *SOMATOTROPIN, *TURNER'S syndrome, *DIAGNOSTIC imaging, *CASTRATION, *GENETICS, *THERAPEUTICS

المؤلفون: Henry, Rohan K.¹ rohan.henry@nationwidechildrens.org, Chaudhari, Monika¹, Bowden, Sasigarn A.¹

المصدر: Clinical Pediatrics. Oct2016, Vol. 55 Issue 11, p1071-1074. 4p.

مصطلحات موضوعية: *TOE abnormalities, *TURNER'S syndrome, *GROWTH disorders, *KARYOTYPES, *FAMILY history (Medicine), *MICROARRAY technology, *ABNORMALITIES in the anatomical extremities, *GENETICS, *DIAGNOSIS

المؤلفون: Ibarra-Ramírez, Marisol¹, Zamudio-Osuna, Michelle Jesús¹, Campos-Acevedo, Luis Daniel¹, Gallardo-Blanco, Hugo Leonid¹, Cerda-Flores, Ricardo Martin², Rodríguez-Sánchez, Irám Pablo¹, Martínez-de-Villarreal, Laura Elia¹

المصدر: Genetic Testing & Molecular Biomarkers. Feb2015, Vol. 19 Issue 2, p88-92. 5p.

مصطلحات موضوعية: *DISEASE prevalence, *TURNER'S syndrome, *SEX chromosome abnormalities, *GENE expression, *POLYMERASE chain reaction, *GENETICS, *DIAGNOSIS

المؤلفون: Denes, Anna-Maria¹, Landin-Wilhelmsen, Kerstin², Wettergren, Yvonne³, Bryman, Inger⁴, Hanson, Charles⁴

المصدر: Genetic Testing & Molecular Biomarkers. Feb2015, Vol. 19 Issue 2, p82-87. 6p.

مصطلحات موضوعية: *DIAGNOSIS of diseases in women, *TURNER'S syndrome, *AGE factors in disease, *DIPLOIDY, *FOLLOW-up studies (Medicine), *FLUORESCENCE in situ hybridization, *GENETICS, *DIAGNOSIS

العنوان البديل: A Rare Karyotype of Turner Syndrome: 45.X/47.XXX.

المؤلفون: Altıncık, Ayça¹, Çatlı, Gönül¹, Demir, Korcan¹, Abacı, Ayhan¹ ayhanabaci@gmail.com, Bora, Elçin², Erçal, Derya², Böber, Ece¹

المصدر: Journal of Current Pediatrics / Guncel Pediatri. 4/1/2014, Vol. 12 Issue 1, p43-47. 5p.

مصطلحات موضوعية: *TURNER'S syndrome, *MITRAL valve insufficiency, *HUMAN growth hormone, *BODY weight, *ECHOCARDIOGRAPHY, *FOLLICLE-stimulating hormone, *INTELLIGENCE tests, *KARYOTYPES, *MENARCHE, *MOSAICISM, *STATURE, *DESCRIPTIVE statistics, *GENOTYPES, *GENETICS, *DIAGNOSIS, *THERAPEUTICS

المؤلفون: Siller, Alejandro F., Shimony, Alex, Shinawi, Marwan, Amarillo, Ina, Dehner, Louis P., Semenkovich, Katherine, Arbeláez, Ana María

المصدر: Journal of Clinical Research in Pediatric Endocrinology; Mar2019, Vol. 11 Issue 1, p88-93, 6p

مصطلحات موضوعية: CHROMOSOME abnormalities, HYPERPARATHYROIDISM, HUMAN growth hormone, CANCER relapse, METASTASIS, PARATHYROID gland tumors, FLUORESCENCE in situ hybridization, TURNER'S syndrome, GENETIC testing, BEHAVIOR disorders, MICROARRAY technology, GENETICS, DIAGNOSIS, THERAPEUTICS

المؤلفون: Zelinska, Nataliya, Shevchenko, Iryna, Globa, Evgenia

المصدر: Journal of Clinical Research in Pediatric Endocrinology; Sep2018, Vol. 10 Issue 3, p256-263, 8p

مصطلحات موضوعية: CHEST abnormalities, NECK abnormalities, BLOOD-vessel abnormalities, CHROMOSOME abnormalities, CRANIOFACIAL dysostosis, GENETIC polymorphisms, GENITOURINARY organ abnormalities, GROWTH disorders, HEARING impaired children, KARYOTYPES, EVALUATION of medical care, NAILS (Anatomy), PREGNANCY, VISION disorders, PHENOTYPES, TURNER'S syndrome, METACARPUS, DISEASE prevalence, RETROSPECTIVE studies, NIPPLE (Anatomy), GENETICS, DIAGNOSIS

مصطلحات جغرافية: UKRAINE

المؤلفون: De Leon, Diva D., Stanley, Charles A.

المصدر: Pediatric Diabetes; Feb2017, Vol. 18 Issue 1, p3-9, 7p

مصطلحات موضوعية: BRAIN diseases, HYPOGLYCEMIA treatment, PANCREATIC physiology, BLOOD sugar, CONFERENCES & conventions, DIURETICS, ENZYMES, GENETIC disorders, INSULIN, EVALUATION of medical care, HYPOGLYCEMIA, MOLECULAR diagnosis, GENETIC mutation, TURNER'S syndrome, DISEASE management, DISEASE complications, GENETICS, DIAGNOSIS, DISEASE risk factors

المؤلفون: Peng, Ruan, Zhou, Yi, Xie, Hong‐Ning, Zheng, Ju, Xie, Ying‐Jun, Yang, Jian‐Bo, Xie, Hong-Ning, Xie, Ying-Jun, Yang, Jian-Bo

المصدر: Prenatal Diagnosis; Aug2016, Vol. 36 Issue 8, p766-774, 9p

مصطلحات موضوعية: HUMAN abnormalities, CHROMOSOME abnormalities, CHROMOSOMES, GENETICS, KARYOTYPES, KLINEFELTER'S syndrome, SECOND trimester of pregnancy, THIRD trimester of pregnancy, PRENATAL diagnosis, TURNER'S syndrome, TWINS, MICROARRAY technology, SYMPTOMS, DIAGNOSIS