Robertsonian translocations - Reproductive risks and indications for preimplantation genetic diagnosis

Human Reproduction

Volumn 16, Issue 11, 2001, Pages 2267-2273

  Scriven, P N ^a   Flinter, F A ^b   Braude, P R ^c   Ogilvie, C Mackie ^a  

^a GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^b Clinical Genetics   (United Kingdom)

^c ST THOMAS HOSPITAL   (United Kingdom)

Author keywords

PGD; Reproductive risks; Robertsonian translocation

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; BIOPSY; CHROMOSOME 10Q; CHROMOSOME ABERRATION; CLINICAL ARTICLE; EMBRYO; EMBRYO TRANSFER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENDER IDENTITY; GENE LOCUS; GENETIC COUNSELING; GENETIC DISORDER; GENETIC SCREENING; HUMAN; INFERTILITY; KARYOTYPE 45,X; MALE; MULTIPLE PREGNANCY; OLIGOSPERMIA; OOCYTE CLEAVAGE; PREGNANCY; PREIMPLANTATION EMBRYO; PRENATAL DIAGNOSIS; REPRODUCTIVE HEALTH; RISK ASSESSMENT; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SEX CHROMOSOME; SEX CHROMOSOME MOSAICISM; SPERMATOZOON COUNT; SPONTANEOUS ABORTION; SUBFERTILITY; TRISOMY 21;

EID: 0035157468     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/16.11.2267     Document Type: Article

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