The incremental yield of CMA over karyotype in fetal ventriculomegaly: a systematic review and meta-analysis. [PDF]
Sapantzoglou I +7 more
europepmc +1 more source
Prenatal diagnosis and genetic counseling of a <i>de novo</i> 16q24.3 microdeletion in a Chinese family. [PDF]
Wu W, Zuo Y, Jin J.
europepmc +1 more source
The Incremental Yield of CMA over Karyotype in Isolated Absent/Hypoplastic Nasal Bone-A Systematic Review and Meta-Analysis. [PDF]
Sapantzoglou I +10 more
europepmc +1 more source
Mosaic Trisomy 14 with Severe Short Stature: A Case Report. [PDF]
Yin C, Ye J, Hou L, Luo X.
europepmc +1 more source
Technological Advances in Molecular Diagnostic Methods for Hereditary Diseases in Preconception and Prenatal Settings. [PDF]
Kong D +5 more
europepmc +1 more source
Case Report: Prenatal clues and postnatal evolution: a case of williams syndrome diagnosed following progressive cardiovascular phenotypes. [PDF]
Zeng Y +7 more
europepmc +1 more source
Fetal Copy Number Variant Detection in Pregnancies with Ultrasound Soft Markers: A Maternal Age-Stratified Retrospective Study. [PDF]
Huang S, Lin L, She L, Liu L, Wu H.
europepmc +1 more source
A fetus with paternal uniparental isodisomy of chromosome 3: genetic analysis and prenatal diagnosis following a positive NIPS with IUGR. [PDF]
Zhang F +5 more
europepmc +1 more source
SNP-Based Chromosomal Microarray Analysis in the Era of Optical Genome Mapping: An Enriched Case-Series Evaluating Copy-Neutral Events. [PDF]
Marr AR, Gonzales PR, Golem S.
europepmc +1 more source
The genetic etiology of spontaneous abortion: insights from chromosomal microarray analysis and whole-exome sequencing. [PDF]
Wang L +5 more
europepmc +1 more source

