The scope, limitations and interpretation of copy number detection in the early embryo using the array CGH technique

Human Reproduction

Volumn 28, Issue 1, 2013, Pages 2-5

  Scriven, Paul N ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; CENTROMERE; CHROMOSOME 22; CHROMOSOME ANALYSIS; CHROMOSOME POSITIONING; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; EMBRYO DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; KARYOTYPING; MOLECULAR IMAGING; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NOTE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84871237886     PISSN: 02681161     EISSN: 14602350     Source Type: Journal    
DOI: 10.1093/humrep/des366     Document Type: Note

References (2)

1. ISCN. In: Shaffer LG, Slovak ML, Campbell LJ (eds). An International System for Human Cytogenetic Nomenclature. Basel: S. Karger, 2009.
2. Mertzanidou A, Wilton L, Cheng J, Spits C, Vanneste E, Moreau Y, Vermeesch JR, Sermon K. Microarray analysis reveals abnormal chromosomal complements in over seventy percent of fourteen normally developing human embryos. Hum Reprod, 2012. doi:10. 1093/humrep/des362.