The causes of misdiagnosis and adverse outcomes in PGD

Human Reproduction

Volumn 24, Issue 5, 2009, Pages 1221-1228

  Wilton, L ^a   Thornhill, A ^b   Traeger Synodinos, J ^c   Sermon, K D ^d   Harper, J C ^e  

^a MELBOURNE IVF   (Australia)

^b London Bridge Associates Ltd   (United Kingdom)

^c UNIVERSITY OF ATHENS   (Greece)

^d VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Allele dropout; Contamination; Misdiagnosis; PGD; Preimplantation genetic screening

Indexed keywords

DNA;

ALLELE; ANEUPLOIDY; ARTICLE; BETA THALASSEMIA; CELL COUNT; CHROMOSOME MOSAICISM; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CONTAMINATION; CUMULUS CELL; CYSTIC FIBROSIS; DELIVERY; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DNA DENATURATION; DNA HYBRIDIZATION; DUCHENNE MUSCULAR DYSTROPHY; EMBRYO; EMBRYO TRANSFER; FAMILIAL AMYLOID POLYNEUROPATHY; FLUORESCENCE IN SITU HYBRIDIZATION; FRAGILE X SYNDROME; GENE MUTATION; GENE PROBE; GENE TRANSLOCATION; GENETIC SCREENING; HEALTH CARE QUALITY; HEMOPHILIA A; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INTRACYTOPLASMIC SPERM INJECTION; LABORATORY DIAGNOSIS; MONOGENIC DISORDER; MYOTONIC DYSTROPHY; POLYMERASE CHAIN REACTION; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; RETINITIS PIGMENTOSA; SEX DETERMINATION; SPERMATOZOON; STANDARDIZATION; TRISOMY 16; TRISOMY 21; UNSAFE SEX; X CHROMOSOME LINKED DISORDER;

EID: 67449116488     PISSN: 02681161     EISSN: 14602350     Source Type: Journal    
DOI: 10.1093/humrep/den488     Document Type: Article

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