UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 187

Sortiert nach

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)

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)

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)

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)

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)

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

The American journal of pathology, 2001-09, Vol.159 (3), p.825-829

2001

Volltextzugriff (PDF)

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome : Further evidence of CHK2 in inherited cancer predisposition

Cancer research (Chicago, Ill.), 2001-08, Vol.61 (15), p.5718-5722

2001

Volltextzugriff (PDF)

Safety issues in assisted reproduction technology: Should ICSI patients have genetic testing before treatment? A practical proposition to help patient information

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

2004

Volltextzugriff (PDF)

The frequency and outcome of breast cancer risk-reducing surgery in finnish BRCA1 and BRCA2 mutation carriers

Scandinavian journal of surgery, 2014-03, Vol.103 (1), p.34-40

2014

Volltextzugriff (PDF)

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

The journal of clinical endocrinology and metabolism, 1996-10, Vol.81 (10), p.3722-3726

1996

Volltextzugriff (PDF)

Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

Nature genetics, 1997-02, Vol.15 (2), p.205-206

1997

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)

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Cell, 1995-09, Vol.82 (6), p.959-968

1995

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)

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)

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)

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer

Carcinogenesis (New York), 2007-05, Vol.28 (5), p.1040-1045

2007

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)

Inhibin: a candidate gene for premature ovarian failure

Human reproduction (Oxford), 2000-12, Vol.15 (12), p.2644-2649

2000

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)

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)

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)

1 – 25 von 187

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(179)
Mit Volltextzugriff
(172)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

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

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

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

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome : Further evidence of CHK2 in inherited cancer predisposition

Safety issues in assisted reproduction technology: Should ICSI patients have genetic testing before treatment? A practical proposition to help patient information

The frequency and outcome of breast cancer risk-reducing surgery in finnish BRCA1 and BRCA2 mutation carriers

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

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

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Breast-Cancer Risk in Families with Mutations in PALB2

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

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

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to 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

Inhibin: a candidate gene for premature ovarian failure

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

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

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

Suchergebnisse filtern