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Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men

Human reproduction (Oxford), 2001-01, Vol.16 (1), p.82-90

2001

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Cancer genetics: estimation of the needs of the population in France for the next ten years

Bulletin du cancer, 2009-09, Vol.96 (9), p.875

2009

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Genetic counselors in France, so what

Gynécologie, obstétrique & fertilité, 2011-10, Vol.39 (10), p.539-540

Thépot, F

2011

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Multicentre approaches to donor insemination in the French CECOS Federation: Nationwide evaluation, donor matching, screening for genetic diseases and consanguinity

Human reproduction (Oxford), 1998-05, Vol.13 (suppl-2), p.35-49

1998

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Pregnancy outcome after artificial insemination or IVF with frozen semen donor: a collaborative study of the French CECOS Federation on 21 597 pregnancies

European journal of obstetrics & gynecology and reproductive biology, 1997-08, Vol.74 (2), p.223-228

1997

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F-017. Gamete donation and autocryopreservation in France during the year 1998

Human reproduction (Oxford), 1999-06, Vol.14 (Suppl_3), p.386-387

Thepot, F.

1999

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The interaction between competition law and corporate governance: opening the 'black box'

Thepot, F C. S

2014

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Informed consent to serum screening for Down syndrome: are women given adequate information?

Prenatal diagnosis, 1999-01, Vol.19 (1), p.1-7

1999

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P54 PGD activity in France: the French specificities

Reproductive biomedicine online, 2010, Vol.20, p.S40-S41

2010

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Oncogénétique: estimation des besoins de la population en France pour les dix ans à venir

Bulletin du cancer, 2009-09, Vol.96 (9), p.875-900

2009

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Maternal serum screening for fetal Down's syndrome, a retrospective study

Clinica chimica acta, 1995-07, Vol.238 (2), p.151-162

1995

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How can the genetic risks of embryo donation be minimized?

Human reproduction (Oxford), 2004-08, Vol.19 (8), p.1685-1688

2004

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Assistance médicale à la procréation : état des pratiques en France: Numéro thématique. Assistance médicale à la procréation

Bulletin epidémiologique hebdomadaire (Paris, France), 2011 (23-24), p.263-265

THEPOT, F

2011

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The presence of alpha-interferon in human amniotic fluid

Journal of general virology, 1982-01, Vol.59 (Pt 2), p.393-396

1982

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Risk of cytomegalovirus transmission by cryopreserved semen: a study of 635 semen samples from 231 donors

Human reproduction (Oxford), 2003-09, Vol.18 (9), p.1881-1886

2003

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Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission

Prenatal diagnosis, 2001-10, Vol.21 (10), p.890-893

2001

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First-trimester prenatal diagnosis of mucolipidosis II (I-cell disease) by chorionic biopsy

American journal of human genetics, 1984-11, Vol.36 (6), p.1379-1389

1984

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P-205. French women undergoing ICSI: a potential role of low-level mosaicism in sex chromosome anomaly in the infertile state?

Human reproduction (Oxford), 1999-06, Vol.14 (Suppl_3), p.243-244

1999

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Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3)

American journal of medical genetics. Part A, 2004-07, Vol.128A (3), p.325-330

2004

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Anomalies génétiques et avortements spontanés à répétition: la part de l’homme

Andrologie (Lille, France), 1996-03, Vol.6 (1), p.24-30

Thepot, F.

1996

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Anomalies génétiques et avortements spontanées à répétition : la part de l'homme : La part du mâle dans les avortements spontanés à répétition

Andrologie (Lille), 1996, Vol.6 (1), p.24-30

THEPOT, F

1996

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Chromosomal prenatal diagnosis: Study of 936 cases of intrauterine abnormalities after ultrasound assessment

Prenatal diagnosis, 1989-04, Vol.9 (4), p.255-269

1989

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Molecular analysis of a ring chromosome X in a family with fragile X syndrome

Human genetics, 1993-10, Vol.92 (4), p.373-378

1993

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Lysosomal hydrolase activity in chorionic villi and embryonic cells in culture

Human genetics, 1985-01, Vol.69 (4), p.378-379

1985

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Multicentre approaches to donor insemination in the French CECOS Federation : Nationwide evaluation, donor matching, screening for genetic diseases and consanguinity . Discussion: Gamete donation: current ethics in the European Union

Human reproduction (Oxford), 1998, Vol.13, p.35-54

1998

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Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men

Cancer genetics: estimation of the needs of the population in France for the next ten years

Genetic counselors in France, so what

Multicentre approaches to donor insemination in the French CECOS Federation: Nationwide evaluation, donor matching, screening for genetic diseases and consanguinity

Pregnancy outcome after artificial insemination or IVF with frozen semen donor: a collaborative study of the French CECOS Federation on 21 597 pregnancies

F-017. Gamete donation and autocryopreservation in France during the year 1998

The interaction between competition law and corporate governance: opening the 'black box'

Informed consent to serum screening for Down syndrome: are women given adequate information?

P54 PGD activity in France: the French specificities

Oncogénétique: estimation des besoins de la population en France pour les dix ans à venir

Maternal serum screening for fetal Down's syndrome, a retrospective study

How can the genetic risks of embryo donation be minimized?

Assistance médicale à la procréation : état des pratiques en France: Numéro thématique. Assistance médicale à la procréation

The presence of alpha-interferon in human amniotic fluid

Risk of cytomegalovirus transmission by cryopreserved semen: a study of 635 semen samples from 231 donors

Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission

First-trimester prenatal diagnosis of mucolipidosis II (I-cell disease) by chorionic biopsy

P-205. French women undergoing ICSI: a potential role of low-level mosaicism in sex chromosome anomaly in the infertile state?

Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3)

Anomalies génétiques et avortements spontanés à répétition: la part de l’homme

Anomalies génétiques et avortements spontanées à répétition : la part de l'homme : La part du mâle dans les avortements spontanés à répétition

Chromosomal prenatal diagnosis: Study of 936 cases of intrauterine abnormalities after ultrasound assessment

Molecular analysis of a ring chromosome X in a family with fragile X syndrome

Lysosomal hydrolase activity in chorionic villi and embryonic cells in culture

Multicentre approaches to donor insemination in the French CECOS Federation : Nationwide evaluation, donor matching, screening for genetic diseases and consanguinity . Discussion: Gamete donation: current ethics in the European Union

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