Results 171 to 180 of about 28,714 (240)

Clinical application of nanopore sequencing for haplotype linkage analysis in preimplantation genetic testing for Duchenne muscular dystrophy. [PDF]

Sci Rep
Xia Q, Chang T, Ding T, Liu Z, Liu J, Li Y, Yao Z.   +6 more
europepmc   +1 more source

Occipital Cephalocele, Polymicrogyria, Ocular Anomaly and Vermian Dysplasia: Prenatal Markers for Knobloch Syndrome. [PDF]

Prenat Diagn
Carmant LS, Miller E, Chitayat D, Hedges S, McGivern B, Harris K, Chong K, Shinar S.   +7 more
europepmc   +1 more source

Risk factors and predisposing conditions for amniotic fluid embolism: a comprehensive review. [PDF]

J Med Life
Timraz JH, Ahmed RA, Metwali NY, Javed Z, Abdelazim S, Farhan R, Yaseen FA, Mansour HA.   +7 more
europepmc   +1 more source

Prenatal Ultrasound Findings and Chromosomal Outcomes of Pregnancies with Mosaic Embryo Transfer. [PDF]

Diagnostics (Basel)
Hong YM, Kim SH, Park HJ, Ryu HM, Cha DH, Kim MY, Han YJ.   +6 more
europepmc   +1 more source

Case Report: A prenatal case with sex discordance between non-invasive prenatal testing and fetal genetic testings due to maternal rare chromosome karyotype. [PDF]

Front Genet
Zhong G, Wu J, Zhong Z, Chen D, Guan Z, Huang S, Chen J.   +6 more
europepmc   +1 more source

Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review. [PDF]

Front Genet
Zhu Y, Wu K, Jiang C, Zhu Q.
europepmc   +1 more source