Rare chromosomal, genetic, and epigenetic-related risks associated with infertility treatment

Seminars in Fetal and Neonatal Medicine

Volumn 19, Issue 4, 2014, Pages 250-253

  Kurinczuk, Jennifer J ^a   Bhattacharya, Siladitya ^b  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF ABERDEEN   (United Kingdom)

Author keywords

ART; Chromosome anomalies; Cystic fibrosis; Genomic imprinting; Health outcomes; Imprinting disorders; IVF; Microdeletions

Indexed keywords

AGENESIS; AZOOSPERMIA; CHROMOSOME ABERRATION; CYSTIC FIBROSIS; EMBRYO DEVELOPMENT; EPIGENETICS; FEMALE; FOLLOW UP; GENOME IMPRINTING; GERM CELL; HUMAN; INFERTILITY THERAPY; INTRACYTOPLASMIC SPERM INJECTION; MALE; MALE INFERTILITY; REVIEW; VAS DEFERENS; Y CHROMOSOME; ADVERSE EFFECTS; GENETIC EPIGENESIS; GENETICS; INFERTILITY, FEMALE; INFERTILITY, MALE;

CHROMOSOME ABERRATIONS; EPIGENESIS, GENETIC; FEMALE; GENOMIC IMPRINTING; HUMANS; INFERTILITY, FEMALE; INFERTILITY, MALE; MALE; REPRODUCTIVE TECHNIQUES, ASSISTED; SPERM INJECTIONS, INTRACYTOPLASMIC;

EID: 84904814145     PISSN: 1744165X     EISSN: 18780946     Source Type: Journal    
DOI: 10.1016/j.siny.2014.04.005     Document Type: Review

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