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Molecular Genetics & Genomic Medicine|November 18, 2022
Estimate of genetic variants using CNV-Seq for fetuses with oligohydramnios or polyhydramniosPanlai Shi, Yaqin Hou, Duo Chen, et al.
Prenatal Diagnosis|June 11, 2024
Prenatal exome sequencing for the morphologically normal fetus: Should we be doing it?Zhi Gao, Xiaofan Zhu, Huanan Ren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 9, 2024
Molecular findings in patients for whole exome sequencing and mitochondrial genome assessmentGege Sun, Wei Huang, Li Wang, et al.
Orphanet Journal of Rare Diseases|April 12, 2024
Genetic analysis of 37 cases with primary periodic paralysis in Chinese patientsXuechao Zhao, Haofeng Ning, Lina Liu, et al.
Cold Spring Harbor Perspectives in Medicine|December 6, 2014
A Review of Secondary Photoreceptor Degenerations in Systemic DiseaseNaveen Mysore, Jamie Koenekoop, Shen Li, et al.
Investigative Ophthalmology & Visual Science|February 14, 2017
The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani FamiliesVafa Keser, Ayesha Khan, Sorath Siddiqui, et al.
American Journal of Obstetrics and Gynecology|January 30, 2023
The uncertainty of copy number variants: pregnancy decisions and clinical follow-upPanlai Shi, Hongbin Liang, Yaqin Hou, et al.
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