A Fetus with Hb Bart’s Disease Due to Maternal Uniparental Disomy for Chromosome 16-Reference-Cited by-同舟云学术

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

Published:2015-11-16 Issue:1 Volume:40 Page:66-69
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Au Patrick K.C.,Kan Anita S.Y.,Tang Mary H.Y.,Leung Kwok Y.,Chan Kelvin Y.K.,Tang Tommy W.F.,Lau Elizabeth T.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1096283

Reference11 articles.

1. Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening

2. Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong

3. Two Unusual Cases of Haemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy or Non-Paternity

4. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

5. Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Inherited Genetic Risk in Stillbirth: A Shared Genomic Segments Analysis of High-Risk Pedigrees.;2024-08-23

2. Uniparental disomy and imprinting disorders;Cases in Laboratory Genetics and Genomics (LGG) Practice;2023

3. 20 years review of antenatal diagnosis of haemoglobin Bart's disease and treatment with intrauterine transfusion;Prenatal Diagnosis;2022-03-08

4. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

5. Germline mosaicism in an α‐thalassemia family: Incidental identification by prenatal ultrasound;Prenatal Diagnosis;2019-08-12

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