nature.com search

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Search
My Account Login

nature
search

advanced

where the list of authors contains where the title contains

Refine your results by…

volume

start page / article no.

Filters

Filter By:

Article type

Check one or more article types to show results from those article types only.

Research (10)

Journal

Check one or more journals to show results from those journals only.

Genetics in Medicine (8)
European Journal of Human Genetics (6)
Nature (1)

Choose more journals

Subject Check one or more subjects to show results from those subjects only.

Chromosome abnormality (1)
Genetic counselling (1)
Genetic techniques (1)
Genetic testing (1)
Inbreeding (1)

Date

Choose a date option to show results from those dates only.

Today
Last 7 days
Last 30 days
In the last year
Last 2 years
Last 5 years

Custom date range

Sort by Relevance

Choose a way to sort results.

Relevance
Date — most recent
Date — oldest first

Loading Filters

Showing 1–15 of 15 results

Loading Filters

17 July 2013
Comment on Gialluisi et al
European Journal of Human Genetics 22 , 157–157

Rights & permissionsfor article Comment on Gialluisi <i>et al</i> . Opens in a new window.
31 May 2006
Segregation ratio in cranio-cerebello-cardiac syndrome
European Journal of Human Genetics 14 , 1054–1057

Rights & permissionsfor article Segregation ratio in cranio-cerebello-cardiac syndrome . Opens in a new window.
9 November 1989
Carrier screening in CF
- LEO P. TEN KATE
Nature 342 , 131–131

Rights & permissionsfor article Carrier screening in CF . Opens in a new window.
Research | 7 August 2013 | Open
Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society
European Journal of Human Genetics 22 , 452–457

Rights & permissionsfor article Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society . Opens in a new window.
6 May 2011
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report
- Hanan Hamamy
- , Stylianos E Antonarakis
- , Luigi Luca Cavalli-Sforza
- , Samia Temtamy
- , Giovanni Romeo
- , Leo P Ten Kate
- , Robin L Bennett
- , Alison Shaw
- , Andre Megarbane
- , Cornelia van Duijn
- , Heli Bathija
- , Siv Fokstuen
- , Eric Engel
- , Joel Zlotogora
- , Emmanouil Dermitzakis
- , Armand Bottani
- , Sophie Dahoun
- , Michael A Morris
- , Steve Arsenault
- , Mona S Aglan
- , Mubasshir Ajaz
- , Ayad Alkalamchi
- , Dhekra Alnaqeb
- , Mohamed K Alwasiyah
- , Nawfal Anwer
- , Rawan Awwad
- , Melissa Bonnefin
- , Peter Corry
- , Lorraine Gwanmesia
- , Gulshan A Karbani
- , Maryam Mostafavi
- , Tommaso Pippucci
- , Emmanuelle Ranza-Boscardin
- , Bruno Reversade
- , Saghira M Sharif
- , Marieke E Teeuw
- & Alan H Bittles
Genetics in Medicine 13 , 841–847

Rights & permissionsfor article Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report . Opens in a new window.
Research | 1 November 2005
Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem
Genetics in Medicine 7 , 605–610

Rights & permissionsfor article Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem . Opens in a new window.
1 July 2002
Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria
Genetics in Medicine 4 , 241–249

Rights & permissionsfor article Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria . Opens in a new window.
Research | 4 May 2005
The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study
European Journal of Human Genetics 13 , 947–952

Rights & permissionsfor article The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study . Opens in a new window.
Research | 1 May 2005
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe
Genetics in Medicine 7 , 302–310

Rights & permissionsfor article Genetic education and nongenetic health professionals: Educational providers and curricula in Europe . Opens in a new window.
Research | 1 February 2008
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 10 , 99–106

Rights & permissionsfor article Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale . Opens in a new window.
Research | 1 May 2005
Are pregnant women making informed choices about prenatal screening?
Genetics in Medicine 7 , 332–338

Rights & permissionsfor article Are pregnant women making informed choices about prenatal screening? . Opens in a new window.
Research | 19 October 2001
A genome-wide scan for preeclampsia in the Netherlands
European Journal of Human Genetics 9 , 758–764

Rights & permissionsfor article A genome-wide scan for preeclampsia in the Netherlands . Opens in a new window.
Research | 1 May 2005
Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation
Genetics in Medicine 7 , 295–301

Rights & permissionsfor article Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation . Opens in a new window.
Research | 1 February 2012
Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism
European Journal of Human Genetics 20 , 729–733

Rights & permissionsfor article Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism . Opens in a new window.
Research | 1 November 2008
Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands
Genetics in Medicine 10 , 820–830

Rights & permissionsfor article Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands . Opens in a new window.

Search

Article Search

Advanced search

Quick links

Explore articles by subject
Find a job
Guide to authors
Editorial policies

nature.com sitemap

About us
Press releases
Press office
Contact us

Discover content

Journals A-Z
Articles by subject
Nano
Protocol Exchange
Nature Index

Publish with us

Guide to Authors
Guide to Referees
Editorial policies
Open access
Reprints & permissions

Researcher services

Research data
Language editing
Scientific editing
Nature Masterclasses
Nature Research Academies

Libraries & institutions

Librarian service & tools
Librarian portal
Open research
Recommend to library

Advertising & partnerships

Advertising
Partnerships & Services
Media kits
Branded content

Career development

Nature Careers
Nature Conferences
Nature events

Regional websites

Nature China
Nature India
Nature Japan
Nature Korea
Nature Middle East

Legal & Privacy

Privacy Policy
Use of cookies
Manage cookies/Do not sell my data
Legal notice
Accessibility statement
Terms & Conditions
California Privacy Statement

Refine your results by…

Filters ​

Filter By:

Search

Quick links

Filters