Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: Where are we now?

Journal of B.U.ON.

Volumn 14, Issue SUPPL.1, 2009, Pages

  Konstantopoulou, Irene ^a   Pertesi, M ^a   Fostira, F ^a   Grivas, A ^b   Yannoukakos, D ^a  

^a INSTITUTE OF NANOSCIENCE AND NANOTECHNOLOGY   (Greece)

^b METAXA CANCER HOSPITAL   (Greece)

Author keywords

APC; BRCA1 and 2; Familial cancer; Hereditary cancer; Lynch syndrome; Preimplantation genetic diagnosis

Indexed keywords

ADENOMATOUS POLYP; BREAST CANCER; CANCER RISK; CANCER SUSCEPTIBILITY; CLINICAL FEATURE; COLORECTAL CANCER; CONFERENCE PAPER; DISEASE COURSE; FAMILIAL CANCER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; HUMAN; NEUROFIBROMATOSIS; OVARY CANCER; POLYMERASE CHAIN REACTION; PREIMPLANTATION GENETIC DIAGNOSIS; PRENATAL DIAGNOSIS; RETINOBLASTOMA; TUBEROUS SCLEROSIS; VON HIPPEL LINDAU DISEASE;

ADULT; CHILD; FEMALE; FERTILIZATION IN VITRO; GENES, DOMINANT; GENES, RECESSIVE; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; NEOPLASMS; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME;

EID: 70350050233     PISSN: 11070625     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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