Zobrazeno 1 - 10
of 1 207
pro vyhledávání: '"Karyotype analysis"'
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Background The 15q11.2 BP1-BP2 microdeletion syndrome is associated with developmental delays, language impairments, neurobehavioral disorders, and psychiatric complications. The aim of the present study was to provide prenatal and postnatal
Externí odkaz:
https://doaj.org/article/02a7f68848f14fb6aa02b4dec588e2b8
Publikováno v:
Zhongguo quanke yixue, Vol 27, Iss 23, Pp 2883-2887 (2024)
Background Chromosomal abnormalities are one of the common causes of birth defects, and karyotype analysis is still an important method for prenatal diagnosis of chromosomal abnormalities as well as an effective way to prevent and control birth defec
Externí odkaz:
https://doaj.org/article/04a0172471da44179c6c770a84d66e0e
Publikováno v:
Xibei zhiwu xuebao, Vol 44, Iss 7, Pp 1122-1128 (2024)
Abstract [Objective] Sagittaria trifolia is an important horticultural and cash crop in China. Identification of genome size and analysis of karyotype are essential for genome research and molecular genetics of S. trifolia. Currently, the genome si
Externí odkaz:
https://doaj.org/article/678c1113bfe642d9bc4f72bc696b7391
Autor:
Yongle Zhang, Peng Fu, Jie Li, Huai Yang, Xioxiao Yi, Zujun Yang, Chen Chen, Feiquan Tan, Jinliang Shen, Peigao Luo
Publikováno v:
HortScience, Vol 59, Iss 10 (2024)
Akebia trifoliata, as a new fruit, is becoming competitive and popular in the markets of eastern Asian countries, especially China, because of its nutritional value and health-promoting functions. To ultimately develop seedless varieties, germinating
Externí odkaz:
https://doaj.org/article/d49ca6a3f2b1432e8c8412673864b696
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Both copy number variant-sequencing (CNV-seq) and karyotype analysis have been used as powerful tools in the genetic aetiology of fetuses with congenital heart diseases (CHD). However, CNV-seq brings clinicians more confusions to
Externí odkaz:
https://doaj.org/article/0bedbde337d7439abecacc145a8e2ba5
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Background Premature ovarian insufficiency (POI) is a clinical condition characterized by ovarian dysfunction in women under 40. The etiology of most POI cases remains unidentified and is believed to be multifactorial, including factors such
Externí odkaz:
https://doaj.org/article/8807c1ab43344c5c86c85f18fbc627e5
Autor:
Yunsheng Ge, Jiayan Chen, Yanru Huang, Di Shao, Wenbo Wang, Meijiao Cai, Meihua Tan, Jian Zhang
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Fetal chromosomal abnormalities are the main cause of adverse pregnancy outcomes and are the focus of invasive prenatal diagnosis. Recent studies have demonstrated that various techniques have distinct advantages. Achieving high-resolution and effect
Externí odkaz:
https://doaj.org/article/81aee62e5a1c4754b05a2e0eb128a48f
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Karyotype analysis and fluorescence in situ hybridization (FISH) are commonly used for prenatal diagnosis, however they have many disadvantages. Chromosome microarray analysis (CMA) has the potential to overcome these disadvantage
Externí odkaz:
https://doaj.org/article/2d374c6ac22b4c6bb6c241b1320fe07e
Autor:
Peiwen Xu, Lijuan Wang, Jing Li, Sexin Huang, Ming Gao, Ranran Kang, Jie Li, Hongqiang Xie, Xiaowei Liu, Junhao Yan, Xuan Gao, Yuan Gao
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-15 (2023)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common autosomal dominant genetic diseases. Whole exome sequencing (WES) is a routine tool for diagnostic confirmation of genetic diseases, and it is usually
Externí odkaz:
https://doaj.org/article/db5322f1f81a46d287c1d2f030dc70cf
Publikováno v:
Guangxi Zhiwu, Vol 43, Iss 10, Pp 1828-1837 (2023)
Salvia is the largest genus of the Lamiaceae. Several species of Salvia are used as traditional Chinese medicine, as well as ornamental species. To explore the evolution pattern of species in Hengduan Mountains at the cytological level and to discuss
Externí odkaz:
https://doaj.org/article/5fe0f668d34648f9b0a7de5b2236a275