PGD for monogenic disorders: Aspects of molecular biology

Prenatal Diagnosis

Volumn 29, Issue 1, 2009, Pages 50-56

  Spits, Claudia ^a,b   Sermon, Karen ^b  

^a UNIVERSITY HOSPITAL BRUSSELS   (Belgium)

^b Department of Embryology and Genetics ^*  (Belgium)

Author keywords

Preimplantation genetic diagnosis; Single cell genetics; Single cell pcr; Whole genome amplification

Indexed keywords

DNA POLYMERASE;

AUTOSOMAL DOMINANT INHERITANCE; BEGINNING OF HUMAN LIFE; BLASTOMERE; CONFERENCE PAPER; CYTOLYSIS; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC TEST; DNA DETERMINATION; DNA MICROARRAY; ETHICAL DECISION MAKING; FERTILIZATION IN VITRO; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE LOCUS; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC VARIABILITY; GENOME ANALYSIS; HETEROZYGOSITY; HUMAN; MOLECULAR BIOLOGY; MONOGENIC DISORDER; MULTIPLEX POLYMERASE CHAIN REACTION; PREIMPLANTATION GENETIC DIAGNOSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ALLELIC IMBALANCE; FEMALE; HUMANS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

EID: 59449087092     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2161     Document Type: Conference Paper

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