Results 1 to 10 of about 568,677 (265)
Background Premature ovarian failure (POF), affecting women under 40, is characterized by early loss of ovarian function with unclear pathogenesis.
Yun Zhang +6 more
doaj +1 more source
Epidemiology of congenital polydactyly and syndactyly in Hunan Province, China
Objective To describe the prevalence and epidemiology of congenital polydactyly and syndactyly in Hunan Province, China, 2016–2020. Methods Data were obtained from the Birth Defects Surveillance System in Hunan Province, China, 2016–2020.
Xu Zhou +10 more
doaj +1 more source
Measuring maternal health: focus on maternal morbidity
A reduction in maternal mortality has traditionally been used as a critical measure of progress in improving maternal health. If a 75% reduction in maternal mortality between 1990 and 2015 – the target set under Millennium Development Goal 5 – is to be attained, we must redouble our efforts.
Firoz, Tabassum +8 more
openaire +4 more sources
To analyze the genotype distribution of human papillomavirus (HPV) infection in women in the Huizhou region of China and determine its correlation with age and degree of cervical lesions, with the aim to understand the characteristics of HPV infection in
Xiaoting Wang +5 more
doaj +1 more source
Objective To analyze the infection status and subtype distribution of high-risk human papillomavirus (hrHPV) and their relationship with cervical lesions among women undergoing cervical cancer screening in Guizhou Province, thereby informing HPV vaccine ...
Xingjing Luo +7 more
doaj +1 more source
Application of chromosomal microarray analysis for fetuses with nasal bone agenesis or hypoplasia
Objective To explore the utility of microarray technology in prenatal diagnosis of nasal bone agenesis or hypoplasia. Methods Between July 2018 to October 2023, several cases of abnormal nasal bone development were diagnosed via ultrasound at county and ...
Keqin Jin +8 more
doaj +1 more source
Identification of EVC variants and the preimplantation genetic testing in a Chinese family
Fetal genetic skeletal disorders are common congenital anomalies with notable genetic and phenotypic heterogeneity. Genetic analysis plays an important role in the definitive diagnosis of these skeletal conditions.
Haiyan Luo +13 more
doaj +1 more source
Application of family whole-exome sequencing for prenatal diagnosis—an analysis of 357 cases
ObjectiveTranslation of fertility risks through whole-exome sequencing of family lines to identify variants that explain patient’s clinical phenotypes.Methods1.
Yijun Ge +10 more
doaj +1 more source

