Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature-Reference-Cited by-同舟云学术

Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature

Published:2014-05 Issue:5 Volume:94 Page:695-709
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ordulu Zehra,Wong Kristen E.,Currall Benjamin B.,Ivanov Andrew R.,Pereira Shahrin,Althari Sara,Gusella James F.,Talkowski Michael E.,Morton Cynthia C.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference44 articles.

1. The chromosome number of man;Tjio;Hereditas,1956

2. A proposed standard system of nomenclature of human mitotic chromosomes (Denver, Colorado);Ann. Hum. Genet.,1960

3. Chemical differentiation along metaphase chromosomes;Caspersson;Exp. Cell Res.,1968

4. Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis;Caspersson;Hereditas,1972

5. Paris Conference (1971): Standardization in human cytogenetics;Cytogenetics,1972

Cited by 45 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. Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders;Human Genetics;2024-07

2. Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangements;2024-06-19

3. The importance of the trisomy 21 local cutoff value evaluation for prenatal screening in the second trimester of pregnancy;Laboratory Medicine;2023-04-13

4. External Quality Assessment of Maternal Serum Levels of Alpha-Fetoprotein, Free Beta-Human Chorionic Gonadotropin, and Unconjugated Estriol in Detecting Down Syndrome and Neural Tube Defects in the Second Trimester of 87 Maternal Serum Samples, Based on 105-139 Days;Medical Science Monitor;2022-02-21

5. Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing;Current Protocols in Human Genetics;2020-12