UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 192

Sortiert nach

Children born after cryopreservation of embryos or oocytes: a systematic review of outcome data

Human reproduction (Oxford), 2009-09, Vol.24 (9), p.2158-2172

2009

Volltextzugriff (PDF)

Breast-Cancer Risk in Families with Mutations in PALB2

The New England journal of medicine, 2014-08, Vol.371 (6), p.497-506

2014

Volltextzugriff (PDF)

Recent developments in genetics and medically assisted reproduction: from research to clinical applications

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.12-33

2018

Volltextzugriff (PDF)

High cyclin B1 expression is associated with poor survival in breast cancer

British journal of cancer, 2009-04, Vol.100 (7), p.1055-1060

2009

Volltextzugriff (PDF)

Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

Clinical genetics, 2018-03, Vol.93 (3), p.595-602

2018

Volltextzugriff (PDF)

The DNA damage signalling kinase ATM is aberrantly reduced or lost in BRCA1 BRCA2-deficient and ER PR ERBB2-triple-negative breast cancer

Oncogene, 2008-04, Vol.27 (17), p.2501-2506

2008

Volltextzugriff (PDF)

Increased risk of cancer in patients with fumarate hydratase germline mutation

Journal of medical genetics, 2006-06, Vol.43 (6), p.523-526

2006

Volltextzugriff (PDF)

Overabundant FANCD2, alone and combined with NQO1, is a sensitive marker of adverse prognosis in breast cancer

Annals of oncology, 2013-11, Vol.24 (11), p.2780-2785

2013

Volltextzugriff (PDF)

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Clinical genetics, 2015-07, Vol.88 (1), p.68-73

2015

Volltextzugriff (PDF)

Anti-Müllerian hormone as a predictor of follicular reserve in ovarian insufficiency: special emphasis on FSH-resistant ovaries

Human reproduction (Oxford), 2012-03, Vol.27 (3), p.854-860

2012

Volltextzugriff (PDF)

Identification of novel mutations in FOXL2 associated with premature ovarian failure

Molecular human reproduction, 2002-08, Vol.8 (8), p.729-733

2002

Volltextzugriff (PDF)

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Journal of medical genetics, 2006-05, Vol.43 (5), p.e18-e18

2006

Volltextzugriff (PDF)

Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy

Gut, 2003-07, Vol.52 (7), p.1025-1029

2003

Volltextzugriff (PDF)

A two-decade experience of head and neck paragangliomas in a whole population-based single centre cohort

European archives of oto-rhino-laryngology, 2015-08, Vol.272 (8), p.2045-2053

2015

Volltextzugriff (PDF)

Effects of Oral and Transdermal Estradiol Administration on Levels of Sex Hormone-Binding Globulin in Postmenopausal Women with and without a History of Intrahepatic Cholestasis of Pregnancy

The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3431-3434

2005

Volltextzugriff (PDF)

Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis

Human reproduction update, 2013-03, Vol.19 (2), p.87-104

2013

Volltextzugriff (PDF)

Obstetric and neonatal complications in pregnancies conceived after oocyte donation: a systematic review and meta‐analysis

BJOG : an international journal of obstetrics and gynaecology, 2017-03, Vol.124 (4), p.561-572

2017

Volltextzugriff (PDF)

Recent developments in genetics and medically-assisted reproduction: from research to clinical applications

Human reproduction open, 2017-01, Vol.2017 (3), p.hox015

2017

Volltextzugriff (PDF)

Variations in the thrombomodulin and endothelial protein C receptor genes in couples with recurrent miscarriage

Human reproduction (Oxford), 2007-03, Vol.22 (3), p.864-868

2007

Volltextzugriff (PDF)

Levels of Serum C-Reactive Protein during Oral and Transdermal Estradiol in Postmenopausal Women with and without a History of Intrahepatic Cholestasis of Pregnancy

The journal of clinical endocrinology and metabolism, 2005-01, Vol.90 (1), p.142-146

2005

Volltextzugriff (PDF)

Obstetric and neonatal outcome after oocyte donation in 106 women with Turner syndrome: a Nordic cohort study

Human reproduction (Oxford), 2013-06, Vol.28 (6), p.1598-1609

2013

Volltextzugriff (PDF)

Safety issues in assisted reproduction technology

Human reproduction (Oxford), 2004-03, Vol.19 (3), p.472-476

2004

Volltextzugriff (PDF)

Blood-derived gene-expression profiling in unravelling susceptibility to recessive disease

Journal of medical genetics, 2007-11, Vol.44 (11), p.718-720

2007

Volltextzugriff (PDF)

Cancer Risk in Young Women at Risk of Hereditary Nonpolyposis Colorectal Cancer: Implications for Gynecologic Surveillance

Gynecologic oncology, 2001-03, Vol.80 (3), p.346-349

2001

Volltextzugriff (PDF)

A population-based study of the incidence of müllerian aplasia in Finland

Fertility and sterility, 2001-09, Vol.76 (3), p.624-625

2001

Volltextzugriff (PDF)

1 – 25 von 192

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(183)
Mit Volltextzugriff
(176)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Children born after cryopreservation of embryos or oocytes: a systematic review of outcome data

Breast-Cancer Risk in Families with Mutations in PALB2

Recent developments in genetics and medically assisted reproduction: from research to clinical applications

High cyclin B1 expression is associated with poor survival in breast cancer

Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

The DNA damage signalling kinase ATM is aberrantly reduced or lost in BRCA1 BRCA2-deficient and ER PR ERBB2-triple-negative breast cancer

Increased risk of cancer in patients with fumarate hydratase germline mutation

Overabundant FANCD2, alone and combined with NQO1, is a sensitive marker of adverse prognosis in breast cancer

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Anti-Müllerian hormone as a predictor of follicular reserve in ovarian insufficiency: special emphasis on FSH-resistant ovaries

Identification of novel mutations in FOXL2 associated with premature ovarian failure

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy

A two-decade experience of head and neck paragangliomas in a whole population-based single centre cohort

Effects of Oral and Transdermal Estradiol Administration on Levels of Sex Hormone-Binding Globulin in Postmenopausal Women with and without a History of Intrahepatic Cholestasis of Pregnancy

Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis

Obstetric and neonatal complications in pregnancies conceived after oocyte donation: a systematic review and meta‐analysis

Recent developments in genetics and medically-assisted reproduction: from research to clinical applications

Variations in the thrombomodulin and endothelial protein C receptor genes in couples with recurrent miscarriage

Levels of Serum C-Reactive Protein during Oral and Transdermal Estradiol in Postmenopausal Women with and without a History of Intrahepatic Cholestasis of Pregnancy

Obstetric and neonatal outcome after oocyte donation in 106 women with Turner syndrome: a Nordic cohort study

Safety issues in assisted reproduction technology

Blood-derived gene-expression profiling in unravelling susceptibility to recessive disease

Cancer Risk in Young Women at Risk of Hereditary Nonpolyposis Colorectal Cancer: Implications for Gynecologic Surveillance

A population-based study of the incidence of müllerian aplasia in Finland

Suchergebnisse filtern