A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization-Reference-Cited by-同舟云学术

A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization

Published:2013 Issue:1 Volume:6 Page:11
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Qi Qingwei,Zhou Xiya,Jiang Yulin,Hao Na,Zhou Jing,Zhang Liang

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Reference29 articles.

1. Comparative Genomic Hybridization in Combination with Flow Cytometry Improves Results of Cytogenetic Analysis of Spontaneous Abortions

2. Cytogenetic Abnormalities in Products of Conception: A Relationship Revisited

3. Prenatal diagnosis using interphase fluorescencein situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature

4. Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

5. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

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