Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations

Prenatal Diagnosis

Volumn 28, Issue 5, 2008, Pages 434-442

  McArthur, S J ^a   Leigh, D ^a   Marshall, J T ^a   Gee, A J ^a   De Boer, K A ^a   Jansen, R P S ^a  

^a Sydney IVF   (Australia)

Author keywords

Blastocyst biopsy; Single gene disorders; Translocations

Indexed keywords

ADULT; ARTICLE; BIOPSY; BLASTOCYST; BLASTOCYST TROPHECTODERM BIOPSY; CHROMOSOME TRANSLOCATION; EMBRYO; EMBRYO TRANSFER; FAMILIAL DISEASE; FEMALE; FERTILIZATION IN VITRO; GENETIC ANALYSIS; HUMAN; INNER CELL MASS; LIVE BIRTH; MAJOR CLINICAL STUDY; MONOGENIC DISORDER; MULTIPLE PREGNANCY; NIDATION; OOCYTE CLEAVAGE; OOCYTE RETRIEVAL; PREGNANCY RATE; PREIMPLANTATION GENETIC DIAGNOSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PREIMPLANTATION DIAGNOSIS; TRANSLOCATION, GENETIC; TROPHOBLASTS;

EID: 44349116887     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1924     Document Type: Article

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