Zobrazeno 1 - 10
of 2 498
pro vyhledávání: '"Chromosomal Abnormality"'
Autor:
Vivi M. Srivastava, Sukesh Chandran Nair, Melvin Joy, Marie-Therese Manipadam, Uday P. Kulkarni, Anup J. Devasia, N.A Fouzia, Anu Korula, Kavitha M. Lakshmi, L. Jeyaseelan, Aby Abraham, Alok Srivastava
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-18 (2024)
Abstract Background The karyotype is a major determinant of prognosis in myelodysplastic syndrome (MDS). Details of the cytogenetic profile of MDS in South Asia are limited because cytogenetic services are not widely available. Methods We performed a
Externí odkaz:
https://doaj.org/article/8c59fcca04984df3b38ee6051ccd4065
Publikováno v:
Journal of Basic and Applied Zoology, Vol 85, Iss 1, Pp 1-12 (2024)
Abstract Background Lysimachia ramosa (Wall. ex Duby) is a traditionally used medicinal plant in Meghalaya, a northeastern state of India. The people use the leaves of the plant to cure gastrointestinal worm infection. Kaempferol derivative, isolated
Externí odkaz:
https://doaj.org/article/e5393d7622894ce38c3ee7767896cdfb
Autor:
Bozhinovski Gj, Terzikj M, Kubelka-Sabit K, Jasar Dz, Lazarevski S, Livrinova V, Plaseska-Karanfilska D
Publikováno v:
Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 11-20 (2024)
Chromosomal abnormalities are the most common causes of early pregnancy losses (EPLs). In this study, we aimed to evaluate the incidence and spectrum of chromosomal abnormalities in EPLs and correlate them with different clinical characteristics. We
Externí odkaz:
https://doaj.org/article/bcee29da2b804827bcaacc2e3dd700af
Autor:
Chih-Ping Chen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 2, Pp 174-177 (2024)
Fetal pleural effusion has been reported to be associated with chromosomal abnormalities, genetic syndromes, obstructive uropathy, lymphatic vessel abnormalities such as Noonan syndrome, RASopathy and congenital lymphatic anomalies, thoracic cavity d
Externí odkaz:
https://doaj.org/article/708507772984474dbd8972ce0bd3f8b5
Autor:
Shiyu Sun, Yizhen Ji, Di Shao, Yasong Xu, Xiaomei Yang, Li Sun, Nan Li, Hui Huang, Qichang Wu
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
This study aimed to assess the efficiency of CNV-seq and WES in detecting genetic cause of congenital heart disease (CHDs) in prenatal diagnoses and to compare CNV detection rate between isolated and non-isolated CHD cases. We conducted a retrospecti
Externí odkaz:
https://doaj.org/article/c937794c9f7046c7815928c9322cdb89
Autor:
Chih-Ping Chen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 2, Pp 165-167 (2024)
Fetal pleural effusion has been reported to be associated with chromosomal abnormalities, genetic syndromes, obstructive uropathy, lymphatic vessel abnormalities such as Noonan syndrome, RASopathy and congenital lymphatic anomalies, thoracic cavity d
Externí odkaz:
https://doaj.org/article/f78514bded634451967f070371bc7598
Autor:
Shaobin Lin, Shanshan Shi, Jian Lu, Zhiming He, Danlun Li, Linhuan Huang, Xuan Huang, Yi Zhou, Yanmin Luo
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-14 (2024)
Abstract Background The contribution of genetic variants to congenital heart defects (CHDs) has been investigated in many postnatal cohorts but described in few prenatal fetus cohorts. Overall, specific genetic variants especially copy number variant
Externí odkaz:
https://doaj.org/article/d2d766d3de7b4b2e8f18ca174b1d69be
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:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundMale sperm DNA fragmentation (SDF) may be associated with assisted reproductive technology (ART) outcomes, but the impact of SDF on the occurrence of aneuploid-related miscarriage remains controversial.MethodsGenome-wide single-nucleotide p
Externí odkaz:
https://doaj.org/article/7dac0b7714704c1e86c9af6c6121fe2d
Publikováno v:
International Journal of Women's Health, Vol Volume 15, Pp 1705-1710 (2023)
Shuyun Zhang,1,* Lijuan Wu,1,* Xue Li,1 Li Yang,1 Sujuan Shen,1 Hong Shen,1 Dan Zhao,2 Lin Qi2,3 1Center of Reproductive Medicine, The Second Affiliated Hospital of Soochow University, Su Zhou, People’s Republic of China; 2Precision Medicin
Externí odkaz:
https://doaj.org/article/c9cc854b9255464e9a3413f76eeb8981