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...

Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion

Fertility and sterility, 2017-01, Vol.107 (1), p.150-159.e2

2017

Volltextzugriff (PDF)

The impact of needs-based education on the change of knowledge and attitudes towards medical genetics in medical students

European journal of human genetics : EJHG, 2021-05, Vol.29 (5), p.726-735

2021

Volltextzugriff (PDF)

Editorial: The Importance of Genetic Literacy and Education in Medicine

Frontiers in genetics, 2022-04, Vol.13, p.910530-910530

2022

Volltextzugriff (PDF)

Matrix metalloproteinase and tissue inhibitors of metalloproteinases gene polymorphisms in disorders that influence fertility and pregnancy complications: A systematic review and meta-analysis

Gene, 2018-03, Vol.647, p.48-60

2018

Volltextzugriff (PDF)

Protective Effect of EBF Transcription Factor 1 ( EBF1 ) Polymorphism in Sporadic and Familial Spontaneous Preterm Birth: Insights from a Case-Control Study

International journal of molecular sciences, 2024-10, Vol.25 (20), p.11192

2024

Volltextzugriff (PDF)

Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch–Boonstra–Schaaf Optic Atrophy Syndrome

Clinical genetics, 2024-12, Vol.106 (6), p.786-787

2024

Volltextzugriff (PDF)

Non-genetic physicians’ knowledge, attitudes and behavior towards medical genetics

Wiener Klinische Wochenschrift, 2024-03, Vol.136 (5-6), p.137-145

2024

Volltextzugriff (PDF)

Surface EMG based muscle fatigue evaluation in biomechanics

Clinical biomechanics (Bristol), 2009-05, Vol.24 (4), p.327-340

2009

Volltextzugriff (PDF)

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

The journal of maternal-fetal & neonatal medicine, 2021-07, Vol.34 (14), p.2221-2226

2021

Volltextzugriff (PDF)

Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages

Frontiers in genetics, 2022-01, Vol.12, p.793834-793834

2022

Volltextzugriff (PDF)

A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion

American journal of reproductive immunology (1989), 2017-12, Vol.78 (6), p.n/a

2017

Volltextzugriff (PDF)

Decoding the Epigenetics of Infertility: Mechanisms, Environmental Influences, and Therapeutic Strategies

Epigenomes, 2024-09, Vol.8 (3), p.34

2024

Volltextzugriff (PDF)

DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking status

Croatian medical journal, 2020-02, Vol.61 (1), p.8-17

2020

Volltextzugriff (PDF)

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion

Reproductive biomedicine online, 2012-05, Vol.24 (5), p.567-575

2012

Volltextzugriff (PDF)

Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth

Biological research for nursing, 2022-01, Vol.24 (1), p.85-93

2022

Volltextzugriff (PDF)

Combination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage

Molecular genetics & genomic medicine, 2019-12, Vol.7 (12), p.e980-n/a

2019

Volltextzugriff (PDF)

Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study

Croatian medical journal, 2020-08, Vol.61 (4), p.338-345

2020

Volltextzugriff (PDF)

A rare Y-autosome translocation found in a patient with nonobstructive azoospermia: Case report

Systems biology in reproductive medicine, 2021-07, Vol.67 (4), p.307-313

2021

Volltextzugriff (PDF)

Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis

Reproductive biomedicine online, 2016-02, Vol.32 (2), p.237-246

2016

Volltextzugriff (PDF)

Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion

Fertility and sterility, 2013-06, Vol.99 (7), p.1923-1929

2013

Volltextzugriff (PDF)

GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

Genes, 2024-02, Vol.15 (2), p.255

2024

Volltextzugriff (PDF)

Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review

Fertility and sterility, 2013-05, Vol.99 (6), p.1663-1667

2013

Volltextzugriff (PDF)

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

Journal of assisted reproduction and genetics, 2017-03, Vol.34 (3), p.365-371

2017

Volltextzugriff (PDF)

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

Journal of assisted reproduction and genetics, 2015-12, Vol.32 (12), p.1789-1794

2015

Volltextzugriff (PDF)

Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: Comments on the article by Pereza et al. [2012]

American journal of medical genetics. Part A, 2015-06, Vol.167A (6), p.1426-1427

2015

Volltextzugriff (PDF)

1 – 25 von 109

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(86)
Mit Volltextzugriff
(94)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(105)
Croatian
(13)
Serbian
(1)
Slowenisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion

The impact of needs-based education on the change of knowledge and attitudes towards medical genetics in medical students

Editorial: The Importance of Genetic Literacy and Education in Medicine

Matrix metalloproteinase and tissue inhibitors of metalloproteinases gene polymorphisms in disorders that influence fertility and pregnancy complications: A systematic review and meta-analysis

Protective Effect of EBF Transcription Factor 1 ( EBF1 ) Polymorphism in Sporadic and Familial Spontaneous Preterm Birth: Insights from a Case-Control Study

Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch–Boonstra–Schaaf Optic Atrophy Syndrome

Non-genetic physicians’ knowledge, attitudes and behavior towards medical genetics

Surface EMG based muscle fatigue evaluation in biomechanics

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages

A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion

Decoding the Epigenetics of Infertility: Mechanisms, Environmental Influences, and Therapeutic Strategies

DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking status

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion

Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth

Combination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage

Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study

A rare Y-autosome translocation found in a patient with nonobstructive azoospermia: Case report

Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis

Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion

GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: Comments on the article by Pereza et al. [2012]

Suchergebnisse filtern