UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Mutations in the protamine 1 gene associated with male infertility

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

2007

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Underlying karyotype abnormalities in IVF/ICSI patients

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

2008

Volltextzugriff (PDF)

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

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

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Syndrome de Klinefelter et conseil génétique

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

SIFFROI, J. P

2001

Volltextzugriff (PDF)

Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

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

2000

Volltextzugriff (PDF)

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

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

2004

Volltextzugriff (PDF)

Lack of submicroscopic rearrangements involving telomeres in reproductive failures

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

2002

Volltextzugriff (PDF)

Y chromosome microdeletions and germinal mosaicism in infertile males

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

2000

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

1 – 25 von 128

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(88)
Mit Volltextzugriff
(111)

Publikationsform

Sprache

Englisch
(78)
Französisch
(50)

Erscheinungsjahr

n.n

Thema

Humans
(72)
Life Sciences & Biomedicine
(61)
Science & Technology
(61)
Male
(52)
Biological And Medical Sciences
(36)
Female
(35)
Obstetrics & Gynecology
(33)
Medical Sciences
(30)
Adult
(26)
Chromosome Aberrations
(25)
Reproductive Biology
(24)
Gynecology. Andrology. Obstetrics
(19)
Karyotyping
(19)
Genetics & Heredity
(17)
Infertility, Male - Genetics
(17)
Pregnancy
(17)
In Situ Hybridization, Fluorescence
(15)
Sciences Biologiques Et Medicales
(15)
Medical Genetics
(12)
Sciences Medicales
(12)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

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

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

Suchergebnisse filtern