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Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.
Chang TY, Chung IF, Wu WJ, Chang SP, Lin WH, Ginsberg NA, Ma GC, Chen M. Chang TY, et al. Among authors: ginsberg na. Diagnostics (Basel). 2020 May 7;10(5):286. doi: 10.3390/diagnostics10050286. Diagnostics (Basel). 2020. PMID: 32392875 Free PMC article.
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
Chen M, Yang YS, Shih JC, Lin WH, Lee DJ, Lin YS, Chou CH, Cameron AD, Ginsberg NA, Chen CA, Lee ML, Ma GC. Chen M, et al. Among authors: ginsberg na. Ultrasound Obstet Gynecol. 2014 Apr;43(4):396-403. doi: 10.1002/uog.12550. Epub 2013 Dec 26. Ultrasound Obstet Gynecol. 2014. PMID: 23828768 Free article.
Prenatal diagnosis of 46,XX male fetuses.
Ginsberg NA, Cadkin A, Strom C, Bauer-Marsh E, Verlinsky Y. Ginsberg NA, et al. Am J Obstet Gynecol. 1999 Apr;180(4):1006-7. doi: 10.1016/s0002-9378(99)70673-3. Am J Obstet Gynecol. 1999. PMID: 10203670
The risk and efficacy of chorionic villus sampling in multiple gestations.
Pergament E, Schulman JD, Copeland K, Fine B, Black SH, Ginsberg NA, Frederiksen MC, Carpenter RJ. Pergament E, et al. Among authors: ginsberg na. Prenat Diagn. 1992 May;12(5):377-84. doi: 10.1002/pd.1970120507. Prenat Diagn. 1992. PMID: 1523205 Clinical Trial.
50 results