ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005

被引：65

作者：

Harper, J. C. ^{[1
]}

de Die-Smulders, C. ^{[2
]}

Goossens, V. ^{[3
]}

Harton, G. ^{[4
]}

Moutou, C. ^{[5
]}

Repping, S. ^{[6
]}

Scriven, P. N. ^{[7
,8
]}

SenGupta, S. ^{[1
]}

Traeger-Synodinos, J. ^{[9
]}

Van Rij, M. C. ^{[2
]}

Viville, S. ^{[5
]}

Wilton, L. ^{[10
]}

Sermon, K. D. ^{[11
]}

机构：

[1] UCL, UCL Ctr PGD, Inst Womens Hlth, London WC1E 6HX, England

[2] Univ Hosp Maastricht, PGD Working Grp Maastricht, Dept Clin Genet, NL-6202 AZ Maastricht, Netherlands

[3] ESHRE, Cent Off, B-1852 Grimbergen, Belgium

[4] Genet & IVF Inst, Fairfax, VA 22031 USA

[5] SIHCUS CMCO, Serv Biol Reprod, F-67303 Schiltigheim, France

[6] Univ Amsterdam, Acad Med Ctr, Ctr Reprod Med, Fertil Lab AI 229, NL-1105 AZ Amsterdam, Netherlands

[7] Guys & St Thomas NHS Fdn Trust, Dept Cytogenet, London SE1 9RT, England

[8] Guys & St Thomas NHS Fdn Trust, Ctr Preimplantat Genet Diag, London SE1 9RT, England

[9] Univ Athens, St Sophia Childrens Hosp, Med Genet Lab, Athens 11527, Greece

[10] Melbourne IVF, Melbourne, Vic 3002, Australia

[11] Univ Ziekenhuis Brussel, Dept Embryol & Genet, VUB & Ctr Med Genet, B-1090 Brussels, Belgium

来源：

HUMAN REPRODUCTION | 2008年 / 23卷 / 04期

关键词：

preimplantation genetic diagnosis; preimplantation genetic screening; fluorescence in situ hybridization; polymerase chain reaction; ESHRE PGD Consortium;

D O I：

10.1093/humrep/dem354

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

The seventh report of the ESHRE PGD Consortium is presented documenting cycles collected for the calendar year 2004 and follow-up of the pregnancies and babies born subsequent to these cycles up to October 2005. Since the beginning of the data collections, there has been a steady increase in the number of cycles, pregnancies and babies reported. For data collection VII, 45 centres have participated, reporting on 3358 cycles to oocyte retrieval (OR), 679 pregnancies and 528 babies born. Five hundred and fifty nine OR were reported for chromosomal abnormalities, 113 OR for sexing for X-linked diseases, 520 OR for monogenic diseases, 2087 OR for PGS, and 79 OR for social sexing. Data VII is compared with the cumulative data for data collections I-VI.

引用

页码：741 / 755

页数：15

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