Outcome of twin babies free of Von Hippel-Lindau disease after a double-factor preimplantation genetic diagnosis: monogenetic mutation analysis and comprehensive aneuploidy screening

Fertility and Sterility

Volumn 91, Issue 3, 2009, Pages 933.e1-933.e7

  Obradors, Albert ^a   Fernández, Esther ^b   Rius, Mariona ^a   Oliver Bonet, Maria ^a   Martínez Fresno, Maria ^b   Benet, Jordi ^a   Navarro, Joaquima ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b HOSPITAL QUIRÓN   (Spain)

Author keywords

aneuploidy; CGH; genetic diagnosis; PGD; VHL

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; BIOPSY; BLASTOMERE; CASE REPORT; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; EMBRYO; FEMALE; FERTILIZATION; GENE; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC SCREENING; HETEROZYGOTE; HUMAN; MALE; NIDATION; PRIORITY JOURNAL; SHORT TANDEM REPEAT; TWINS; VON HIPPEL LINDAU DISEASE;

EID: 61349090431     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2008.11.013     Document Type: Article

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