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...

Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening

Journal of genetic counseling, 2004-02, Vol.13 (1), p.31-44

2004

Volltextzugriff (PDF)

Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

European journal of medical genetics, 2013-05, Vol.56 (5), p.243-244

2013

Volltextzugriff (PDF)

Genetics Education for Non-Genetic Health Care Professionals in the Netherlands (2002)

Community genetics, 2006-01, Vol.9 (4), p.246-250

2006

Volltextzugriff (PDF)

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

Molecular human reproduction, 2004-08, Vol.10 (8), p.589-598

2004

Volltextzugriff (PDF)

A genome-wide scan for preeclampsia in the Netherlands

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.758-764

2001

Volltextzugriff (PDF)

Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial

Prenatal diagnosis, 2006-04, Vol.26 (4), p.354-361

2006

Volltextzugriff (PDF)

Discharge and Farewell

Community genetics, 2008-01, Vol.11 (6), p.312-312

ten Kate, Leo P.

2008

Volltextzugriff (PDF)

Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation

Genetics in medicine, 2005-05, Vol.7 (5), p.295-301

2005

Volltextzugriff (PDF)

Does informed decision making influence psychological outcomes after receiving a positive screening outcome?

Prenatal diagnosis, 2009-03, Vol.29 (3), p.271-273

2009

Volltextzugriff (PDF)

Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

Genetics in medicine, 2008-02, Vol.10 (2), p.99-106

2008

Volltextzugriff (PDF)

Editorial: genetic aspects of preconception consultation in primary care

Journal of community genetics, 2012-07, Vol.3 (3), p.155-157

2012

Volltextzugriff (PDF)

Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes

Journal of community genetics, 2010-03, Vol.1 (1), p.37-40

2010

Volltextzugriff (PDF)

Genetic education and nongenetic health professionals: Educational providers and curricula in Europe

Genetics in medicine, 2005-05, Vol.7 (5), p.302-310

2005

Volltextzugriff (PDF)

Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia

American journal of obstetrics and gynecology, 2001-02, Vol.184 (3), p.394-402

2001

Volltextzugriff (PDF)

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

BMC family practice, 2012-10, Vol.13 (1), p.105, Article 105

2012

Volltextzugriff (PDF)

The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study

European journal of human genetics : EJHG, 2005-08, Vol.13 (8), p.947-952

2005

Volltextzugriff (PDF)

The journal of community genetics

Journal of community genetics, 2010-03, Vol.1 (1), p.1-2

2010

Volltextzugriff (PDF)

Does offering and performing prenatal screening influence women's attachment to their unborn child? A longitudinal randomized controlled trial

Prenatal diagnosis, 2007-08, Vol.27 (8), p.757-764

2007

Volltextzugriff (PDF)

Community genetics. Its definition 2010

Journal of community genetics, 2010-03, Vol.1 (1), p.19-22

2010

Volltextzugriff (PDF)

TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

Journal of medical genetics, 2010-06, Vol.47 (6), p.421-428

2010

Volltextzugriff (PDF)

Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden

Midwifery, 2009-10, Vol.25 (5), p.483-499

2009

Volltextzugriff (PDF)

Community Genetics: A Bridge between Clinical Genetics and Public Health

Community genetics, 2005-01, Vol.8 (1), p.7-11

ten Kate, Leo P.

2005

Volltextzugriff (PDF)

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

Genetics in medicine, 2002-07, Vol.4 (4), p.241-249

2002

Volltextzugriff (PDF)

General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices

Journal of community genetics, 2010-06, Vol.1 (2), p.83-90

2010

Volltextzugriff (PDF)

Segregation ratio in cranio-cerebello-cardiac syndrome

European journal of human genetics : EJHG, 2006-09, Vol.14 (9), p.1054-1057

2006

Volltextzugriff (PDF)

26 – 50 von 154

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(127)
Mit Volltextzugriff
(130)

Publikationsform

Artikel
(150)
Buchkapitel
(4)

Sprache

Englisch
(154)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening

Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

Genetics Education for Non-Genetic Health Care Professionals in the Netherlands (2002)

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

A genome-wide scan for preeclampsia in the Netherlands

Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial

Discharge and Farewell

Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation

Does informed decision making influence psychological outcomes after receiving a positive screening outcome?

Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

Editorial: genetic aspects of preconception consultation in primary care

Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes

Genetic education and nongenetic health professionals: Educational providers and curricula in Europe

Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study

The journal of community genetics

Does offering and performing prenatal screening influence women's attachment to their unborn child? A longitudinal randomized controlled trial

Community genetics. Its definition 2010

TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden

Community Genetics: A Bridge between Clinical Genetics and Public Health

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices

Segregation ratio in cranio-cerebello-cardiac syndrome

Suchergebnisse filtern