Celebrating preimplantation genetic diagnosis of p53 mutations in Li-Fraumeni syndrome

Reproductive BioMedicine Online

Volumn 3, Issue 1, 2001, Pages 2-3

  Simpson, Joe Leigh ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

allele drop out; human embryo; human genetics; Li Fraumeni syndrome; p53 mutation; PGD

Indexed keywords

PROTEIN P53;

BREAST CANCER; COLON POLYPOSIS; FAMILIAL CANCER; GENE MUTATION; HUMAN; MARFAN SYNDROME; MENTAL DEFICIENCY; MOLECULAR DIAGNOSIS; NOTE; PREIMPLANTATION GENETIC DIAGNOSIS; RHABDOMYOSARCOMA; STOMACH CANCER;

EID: 85006324011     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/S1472-6483(10)61953-0     Document Type: Note

References (4)

1. Malkin, D, Li-Fraumeni syndrome. Scriver, CR, et al. (eds.) The Metabolic and Molecular Bases of Inherited Disease, 8th edition, 2001, McGraw-Hill, New York, USA, 849–863.
2. Simpson, JL, Carson, S, The reproductive option of sex selection. Human Reproduction 14 (1999), 870–872.
3. Verlinsky, Y, Kuliev, A, An Atlas of Preimplantation Genetic Diagnosis, 2000, Parthenon, New York and London, 174.
4. Verlinsky, Y, Rechitsky, S, Verlinsky, O, et al. Preimplantation diagnosis for p53 tumour suppressor gene mutations. Reproductive BioMedicine Online 2 (2001), 102–105.