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Causes rares d’anomalies de l’empreinte parentale entraînant un retard de croissance à début intra-utérin (RCIU)

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.318-318

2016

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Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

The journal of clinical endocrinology and metabolism, 2016-05, Vol.101 (5), p.2099-2104

2016

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O01 Obtention d’adipocytes beiges humains fonctionnels in vitro et in vivo à partir de cellules souches à pluripotence induite

Diabetes & metabolism, 2015-03, Vol.41, p.A1-A1

2015

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Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation

Human reproduction (Oxford), 2011-03, Vol.26 (3), p.724-728

2011

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Stratégies reproductives et transmission des gènes: grâce aux femmes et malgré les hommes ?

Basic and clinical andrology, 2010-03, Vol.20 (1), p.86-91

Siffroi, J.-P.

2010

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Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

Clinical genetics, 2017-11, Vol.92 (5), p.556-558

2017

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Identification of transcripts by macroarrays, RT–PCR and in situ hybridization in human ejaculate spermatozoa

Molecular human reproduction, 2005-02, Vol.11 (2), p.133-140

2005

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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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Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome

Human reproduction (Oxford), 2020-10, Vol.35 (10), p.2391-2398

2020

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Mutations in the protamine 1 gene associated with male infertility

Molecular human reproduction, 2007-07, Vol.13 (7), p.461-464

2007

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Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study

Human reproduction (Oxford), 2005-03, Vol.20 (3), p.736-740

2005

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Underlying karyotype abnormalities in IVF/ICSI patients

Reproductive biomedicine online, 2008, Vol.16 (4), p.514-522

2008

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Quality assessment of induced spermatogenesis in hypogonadotrophic hypogonadic men treated with gonadotrophins

Reproductive biomedicine online, 2011-03, Vol.22 (3), p.277-283

2011

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Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26

Molecular human reproduction, 2006-10, Vol.12 (10), p.643-646

2006

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Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility

Molecular human reproduction, 2007-01, Vol.13 (1), p.55-59

2007

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Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma

Human reproduction (Oxford), 2018-08, Vol.33 (8), p.1408-1416

2018

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A high frequency of Y chromosome deletions in males with nonidiopathic infertility

The journal of clinical endocrinology and metabolism, 1999-10, Vol.84 (10), p.3606-3612

1999

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Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis

American journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1510-1514

2010

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Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses

Journal of medical genetics, 2002-07, Vol.39 (7), p.514-518

2002

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Syndrome de Klinefelter et conseil génétique

Andrologie (Lille), 2001-03, Vol.11 (1), p.9-14

SIFFROI, J. P

2001

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Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

Molecular human reproduction, 2000-04, Vol.6 (4), p.298-302

2000

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L’avenir de la cytogénétique après le séquencage du génome humain

Morphologie, 2004-04, Vol.88 (280), p.19-23

2004

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Lack of submicroscopic rearrangements involving telomeres in reproductive failures

Human reproduction (Oxford), 2002-05, Vol.17 (5), p.1154-1157

2002

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Y chromosome microdeletions and germinal mosaicism in infertile males

Molecular human reproduction, 2000-08, Vol.6 (8), p.688-693

2000

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Stratégies reproductives et transmission des gènes: grâce aux femmes et malgré les hommes ?: Procréer par don de spermatozoïdes avec ou sans anonymat

Andrologie (Lille, France), 2010, Vol.20 (1), p.86-91

SIFFROI, J.-P

2010

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Causes rares d’anomalies de l’empreinte parentale entraînant un retard de croissance à début intra-utérin (RCIU)

Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

O01 Obtention d’adipocytes beiges humains fonctionnels in vitro et in vivo à partir de cellules souches à pluripotence induite

Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation

Stratégies reproductives et transmission des gènes: grâce aux femmes et malgré les hommes ?

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

Identification of transcripts by macroarrays, RT–PCR and in situ hybridization in human ejaculate spermatozoa

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

Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome

Mutations in the protamine 1 gene associated with male infertility

Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study

Underlying karyotype abnormalities in IVF/ICSI patients

Quality assessment of induced spermatogenesis in hypogonadotrophic hypogonadic men treated with gonadotrophins

Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26

Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility

Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma

A high frequency of Y chromosome deletions in males with nonidiopathic infertility

Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis

Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses

Syndrome de Klinefelter et conseil génétique

Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

L’avenir de la cytogénétique après le séquencage du génome humain

Lack of submicroscopic rearrangements involving telomeres in reproductive failures

Y chromosome microdeletions and germinal mosaicism in infertile males

Stratégies reproductives et transmission des gènes: grâce aux femmes et malgré les hommes ?: Procréer par don de spermatozoïdes avec ou sans anonymat

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