| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8784587 | Taiwanese Journal of Obstetrics and Gynecology | 2017 | 4 Pages |
Abstract
Fetuses with an interstitial deletion of 2q31.1-q32.1 may be associated with increased first-trimester NT. Haploinsufficiency of HOXD13 is associated with syndactyly. Genomic microarray is useful in detecting subtle chromosomal abnormalities in fetuses with increased NT and normal karyotype.
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Authors
Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, Wayseen Wang,