Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong-Reference-Cited by-同舟云学术

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Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong

Published:2019-03-23 Issue: Volume: Page:
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Cheng Shirley S. W.¹^ORCID,Chan Kelvin Y. K.²,Leung Kelphen K. P.¹,Au Patrick K. C.²,Tam Wai‐Keung²,Li Samuel K. M.²,Luk Ho‐Ming¹,Kan Anita S. Y.³,Chung Brian H. Y.⁴⁵,Lo Ivan F. M.¹,Tang Mary H. Y.⁴

Affiliation:

1. Department of HealthClinical Genetic Service Hong Kong

2. Prenatal Diagnostic LaboratoryTsan Yuk Hospital Hong Kong

3. Department of Obstetrics and GynaecologyQueen Mary Hospital Hong Kong

4. Department of Obstetrics and GynaecologyLi Ka Shing Faculty of Medicine, University of Hong Kong Hong Kong HKSAR

5. Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of MedicineUniversity of Hong Kong Hong Kong HKSAR

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31697

Reference58 articles.

1. Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients

2. Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada

3. A Fetus with Hb Bart’s Disease Due to Maternal Uniparental Disomy for Chromosome 16

4. Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-Analysis

5. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

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1. Chromosomal abnormalities detected by chromosomal microarray analysis and pregnancy outcomes of 4211 fetuses with high-risk prenatal indications;Scientific Reports;2024-07-10

2. Konjenital Anomali ve/veya Nörogelişimsel Geriliği olan Çocukluk Çağındaki Türk Hastalarda Kromozomal Mikroarray Deneyimi: ASXL2 Gen Duplikasyonu ve Xq13 Delesyonunun İncelenmesi;Dicle Tıp Dergisi;2024-03-14

3. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD;Scientific Reports;2024-02-14

4. Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study;BMC Pregnancy and Childbirth;2024-01-03

5. Prenatal Utility of Chromosomal Microarray Analysis and Pregnancy Outcomes ： A Cohort Study of 4211 Pregnancies;2024-01-03

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