Found: 8
Select item for more details and to access through your institution.
Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Application of high resolution SNP arrays in patients with congenital oral clefts in south China.
- Published in:
- Journal of Genetics, 2016, v. 95, n. 4, p. 801, doi. 10.1007/s12041-016-0696-0
- By:
- Publication type:
- Article
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.
- Published in:
- Human Genetics, 2021, v. 140, n. 2, p. 333, doi. 10.1007/s00439-020-02200-z
- By:
- Publication type:
- Article
De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl With Developmental Delay, Speech Delay, Congenital Cleft Palate, and Bilateral Hearing Impairment.
- Published in:
- Cleft Palate Craniofacial Journal, 2017, v. 54, n. 3, p. 343, doi. 10.1597/15-171
- By:
- Publication type:
- Article
All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway.
- Published in:
- Journal of Cellular Biochemistry, 2020, v. 121, n. 11, p. 4386, doi. 10.1002/jcb.29659
- By:
- Publication type:
- Article
Prenatal exome sequencing in fetuses with callosal anomalies.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 6, p. 744, doi. 10.1002/pd.6107
- By:
- Publication type:
- Article
Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 10, p. 1290, doi. 10.1002/pd.5737
- By:
- Publication type:
- Article
Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2.
- Published in:
- Molecular Neurobiology, 2023, v. 60, n. 6, p. 2986, doi. 10.1007/s12035-023-03239-5
- By:
- Publication type:
- Article