Treatment of Epilepsy Associated with Common Chromosomal Developmental Diseases by Budisteanu Magdalena, Jurca Claudia, Papuc Sorina Mihaela, Focsa Ina, Riga Dan, Riga Sorin, Jurca Alexandru, Arghir Aurora

Subjects: “…chromosomal diseases…”
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A case report of Williams syndrome with main clinical manifestation of hypercalcemia and gastrointestinal bleeding as the main clinical manifestations, and with an accompanying lit... by Hong Meng, Yue‐Xin Jia, Hui‐Min Yang, Xin Gao, Cha‐Gan‐Hu Li, Guo‐Yan Xin, Yu‐Min Wang

Subjects: “…chromosomal diseases…”
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Análisis de la cinematografía del síndrome de Down by Jose Coronel-Hidalgo, Gabriela Cevallos-Solorzano, Ariana Torres-Galarza, Natalia Bailón-Moscoso

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CLASSIFICATION OF HEREDITARY DISEASES (LECTURE) by Elena A. Tkachuk, Igor Zh. Seminsky

Subjects: “…genetics, classification in genetics, gene diseases, chromosomal diseases, multifactorial diseases…”
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22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT by Leyla S. Namazova-Baranova, Olga V. Ginter, Tatyana A. Polunina, Irina V. Davydova, Kirill V. Savostyanov, Alexandr A. Pushkov, Natalya V. Jourkova, Tatyana Y. Mospan

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Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis by Jinman Zhang, Xinhua Tang, Jilin Hu, Guilin He, Jian Wang, Yingting Zhu, Baosheng Zhu

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A case of 15q11‐q13 duplication syndrome and literature review by Zhuo Fu, Yue‐Xin Jia, Jun‐Xian Fu, Tian‐Xia Li, Jing‐Jing Zhao, Ting Wang, Zhi‐Dong Qiao, Xiao‐Yang Liu, Rong Tang, Ting Lv, Guang‐Lu Yang

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Drug-resistant epilepsy cases in chromosomal pathology by L. B. Novikova, A. P. Akopyan, R. F. Latypova, N. M. Faizullina

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Primary alveolar hypoventilation and XXXXY chromosopathy by D. Samolski, A. Antón, M. Mayos, M. Subirana, R. Güell

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Prenatal Invasive Diagnosis with Quantitative Fluorescent PCR by V. V. Avrutskaja, N. V. Kriventsova, R. A. Shokarev, V. S. Gimbut, S. Y. Kriger

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Congenital Cutis Verticis Gyrata in a Newborn with Turner Syndrome: A Rare Clinical Manifestation of This Chromosomal Disease with Trichoscopic Evaluation by Riccardo Bortone, Domenico Bonamonte, Gerardo Cazzato, Carmelo Laface, Alberto Gaeta, Teresa Lettini, Caterina Foti, Raffaele Filotico, Francesca Ambrogio

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22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment by Leyla S. Namazova-Baranova, Olga V. Ginter, Tatyana A. Polunina, Irina V. Davydova, Kirill V. Savostyanov, Alexandr A. Pushkov, Natalya V. Jourkova, Tatyana Y. Mospan

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Caregivers’ experience of having a child with Down syndrome: a meta-synthesis by Xiao Nan Zhang, Shuo Zhang, Chun Yan Liu, Zhi Hong Ni, Hai Tao Lv

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