Zobrazeno 1 - 10
of 529
pro vyhledávání: '"Chromosomal Disorders"'
Publikováno v:
Majallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, Vol 26, Iss 4, Pp 36-45 (2023)
Introduction: Regarding to the importance of the main role of ultrasonography in screening of chromosomal disorders, the present study was performed with aim to evaluate the relationship between NFT and PT in fetuses of second trimester of pregnancy;
Externí odkaz:
https://doaj.org/article/301dadd56c29488c8961ae8e213e2e47
Autor:
Malak Abedalthagafi, Shahad Bawazeer, Romy I. Fawaz, A. Merrihew Heritage, Nouf M. Alajaji, Eissa Faqeih
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Non-invasive prenatal testing (NIPT) is a pioneering technique that has consistently advanced the field of prenatal testing to detect genetic abnormalities and conditions with the aim of decreasing the incidence and prevalence of inherited conditions
Externí odkaz:
https://doaj.org/article/dbeca6cb54fe4f88ba38268a35274b19
Publikováno v:
JA Clinical Reports, Vol 8, Iss 1, Pp 1-3 (2022)
Abstract Background Monosomy 21 is a rare chromosomal abnormality. It is mainly associated with mental retardation, intellectual disability, growth retardation, microcephaly, and characteristic facial features. General anesthesia in adults with this
Externí odkaz:
https://doaj.org/article/ba590cddc7d144f79e5beb8ae3a526c0
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 10 (2021)
Background: Turner syndrome (TS), also known as 45,X, is a genetic disorder caused by the partial or complete lack of an X chromosome. TS can cause a variety of medical and developmental conditions. We aimed to investigate TS mosaicism and variants p
Externí odkaz:
https://doaj.org/article/6bc98565e4d94f15b8d11e509637457b
Publikováno v:
Gomal Journal of Medical Sciences, Vol 17, Iss 2, Pp 42-46 (2019)
Background: Intellectual disability (ID) is a neuro-developmental defect that is manifested by development delay and learning disability. Such defects may be caused due to chromosomal disorders (trisomy 18 or Down syndrome) or single gene mutation. I
Externí odkaz:
https://doaj.org/article/3e1d041f8d7d467ea403b1f19ccb2cf9
Autor:
James A. Thompson
Publikováno v:
BMC Medical Research Methodology, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Multiple neonatal and pediatric disorders have been linked to older paternal ages. Combining these findings with the evidence that many men are having children at much later ages generates considerable public health concern. The r
Externí odkaz:
https://doaj.org/article/5d17264335264402bf4a359132171668
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Akademický článek
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Akademický článek
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Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 25, Iss 1, Pp 4-6 (2019)
Objective: Cystic hygromas of nuchal origin are reported to be associated with fetal aneuploidy and structural anomalies in 50-80% of the cases. We aimed to report our experience on cystic hygromas via 18 cases. Study Design: We conducted a retrospe
Externí odkaz:
https://doaj.org/article/bd34d79a1f4d4d75b87f4a9a0732ab58