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Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

Apessos, A; Abou-Sleiman, PM; Harper, JC; Delhanty, JDA; (2001) Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers. PRENATAL DIAGNOSIS , 21 (6) pp. 504-511. 10.1002/pd.111.

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Type: Article
Title: Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers
DOI: 10.1002/pd.111
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, Obstetrics & Gynecology, fragile X syndrome, preimplantation genetic diagnosis, single cell PCR, linked polymorphisms, PREMATURE OVARIAN FAILURE, DINUCLEOTIDE REPEAT, CLINICAL-APPLICATION, PCR ANALYSIS, FMR1 GENE, DNA, METHYLATION, INSTABILITY, PREMUTATION, AMELOGENIN
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Inst for Women's Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Inst for Women's Health > Reproductive Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health
URI: http://discovery.ucl.ac.uk/id/eprint/25962
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