ESHRE Preimplantation Genetic Diagnosis Consortium: Data collection III (May 2001)

Human Reproduction

Volumn 17, Issue 1, 2002, Pages 233-246

  Sermon, Karen ^a   Harper, Joyce ^b   Geraedts, Joep ^c   De Die Smulders, Christine ^c   Handyside, Alan ^d   Hussey, Nicole ^e   Magli, Maria Christina ^f   Munné, Santiago ^g   Ray, Pierre ^h   Santalo, Josep ⁱ   Staessen, Catherine ^a   Thornhill, Alan ^j   Viville, Stéphane ^k   Wilton, Leeanda ^l  

^a VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c MAASTRICHT UNIVERSITY   (Netherlands)

^d UNIVERSITY OF LEEDS   (United Kingdom)

^e UNIVERSITY OF ADELAIDE   (Australia)

^f SISMER   (Italy)

^g SAINT BARNABAS MEDICAL CENTER   (United States)

^h HÔPITAL NECKER ENFANTS MALADES   (France)

ⁱ UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^j MAYO CLINIC   (United States)

^k INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^l MELBOURNE IVF   (Australia)

more..

Author keywords

Consortium data collection; FISH; Gender screening; PCR; PDG

Indexed keywords

ANEUPLOIDY; ARTICLE; DATA ANALYSIS; ETHICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENDER; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; LONG TERM CARE; MAJOR CLINICAL STUDY; MEDICAL EDUCATION; MEDICAL RESEARCH; MEDICAL SOCIETY; OOCYTE DEVELOPMENT; OUTCOMES RESEARCH; PATIENT REFERRAL; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION EMBRYO; PRENATAL DIAGNOSIS;

EID: 0001043863     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

1. Preimplantation genetic diagnosis of the fragile X syndrome by use of polymorphic linked markers
2. Seven years of intracytoplasmic sperm injection and follow-up of 1987 subsequent children
3. Multiplex PCR of polymorphic markers flanking the CFTR gene: A general approach for preimplantation genetic diagnosis of cystic fibrosis
4. ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: Preliminary assessment of data from January 1997 to September 1998
5. ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: Data collection II (May 2000)
6. Sex selection and preimplantation genetic diagnosis
7. Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: Identification of the categories for which it should be proposed
8. Clinical application of preimplantation genetic diagnosis for cystic fibrosis
9. Diagnosis of sex in preimplantation embryos by fluorescence in situ hybridization
10. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification
11. Congenital malformations
12. Pregnancies after cryopreservation of embryos biopsied for PGD
13. Impact of blastomere biopsy and cryopreservation techniques on human embryo viability
14. Diagnosis of major chromosome aneuploidies in human preimplantation embryos
15. Outcome of preimplantation genetic diagnosis of translocations
16. A successful strategy for preimplantation genetic diagnosis of myotonic dystrophy using multiplex fluorescent PCR
17. Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the ΔF508 deletion causing cystic fibrosis in clinical practice
18. The place of social sexing in medicine and science
19. Chromosome translocations: Segregation modes and strategies for preimplantation genetic diagnosis
20. Premature ovarian failure in the Fragile X syndrome
21. Clinical experience of sex determination by fluorescent in situ hybridization for preimplantation genetic diagnosis
22. Karyotyping of human oocytes by chromosomal analysis of the second polar body
23. Use of comparative genomic hybridization to karyotype embryos prior to implantation: The achievement of a successful pregnancy