26 results on '"Kan, Anita S. Y."'
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2. Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers
3. Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes
4. Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept
5. Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia
6. Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
7. Additional file 1 of Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes
8. Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications
9. Pregnancies with positive non-invasive prenatal testing result for sex chromosome abnormalities in a tertiary hospital in Hong Kong.
10. Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases
11. The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes
12. Optimal timing of hepatitis B virus DNA quantification and clinical predictors for higher viral load during pregnancy
13. Prenatal diagnosis of 5p deletion syndrome: Report of five cases
14. Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong
15. First Report of a Novel Deletion Due toεγδβ-Thalassemia in a Chinese Family
16. An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
17. The Clinical Impact of Chromosomal Microarray on Paediatric Care in Hong Kong
18. First Report of a Novel Deletion Due to εγδβ -Thalassemia in a Chinese Family.
19. Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong
20. Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early-onset preeclampsia.
21. A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.
22. Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.
23. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
24. A prenatal case of split-hand malformation associated with 17p13.3 triplication - a dilemma in genetic counseling.
25. Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: report and a review of literature.
26. A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12-20 weeks gestation.
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