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BINOCAR

Exact phrase matches only. British and Irish Network of. We are a group of researchers who work closely with several congenital anomaly registers across the United Kingdom, the Republic of Ireland and the European Union. This website, in partnership with EUROCAT,. Provides information and resources for researchers, health professionals, parents and other members of the public. What is a congenital anomaly? BINOCARD - The British and Irish Network of Congenital Anomaly Research Database.

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CONTACTS AT BINOCAR.ORG

Biomedical Computing Ltd

James Densem

Innova●●●●●●Centre

St Leo●●●●●●on-sea , East Sussex, TN38 9UH

GB

44.1●●●●8150
ja●●●@bio-medical.co.uk

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Biomedical Computing Ltd

James Densem

Innova●●●●●●Centre

St Leo●●●●●●on-sea , East Sussex, TN38 9UH

GB

44.1●●●●8150
ja●●●@bio-medical.co.uk

View this contact

Biomedical Computing Ltd

James Densem

Innova●●●●●●Centre

St Leo●●●●●●on-sea , East Sussex, TN38 9UH

GB

44.1●●●●8150
ja●●●@bio-medical.co.uk

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Exact phrase matches only. British and Irish Network of. We are a group of researchers who work closely with several congenital anomaly registers across the United Kingdom, the Republic of Ireland and the European Union. This website, in partnership with EUROCAT,. Provides information and resources for researchers, health professionals, parents and other members of the public. What is a congenital anomaly? BINOCARD - The British and Irish Network of Congenital Anomaly Research Database.
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2 congenital anomaly researchers
3 about us
4 data sources
5 research database binocard
6 eurocat
7 our research
8 events
9 news archive
10 external links
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BINOCAR | binocar.org Reviews

https://binocar.org

Exact phrase matches only. British and Irish Network of. We are a group of researchers who work closely with several congenital anomaly registers across the United Kingdom, the Republic of Ireland and the European Union. This website, in partnership with EUROCAT,. Provides information and resources for researchers, health professionals, parents and other members of the public. What is a congenital anomaly? BINOCARD - The British and Irish Network of Congenital Anomaly Research Database.

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binocar.org binocar.org
1

BINOCAR

http://www.binocar.org/content/Executive

Exact phrase matches only. British and Irish Network of. We are a group of. Regional and disease-specific registers collecting information about congenital anomalies occurring in the United Kingdom and the Republic of Ireland. This website provides information for health professionals, parents and other members of the public, in partnership with EUROCAT. What is a congenital anomaly? See all forthcoming events. CARIS publishes revised table on rare diseases. Website created and hosted by.

2

BINOCAR

http://www.binocar.org/links

Exact phrase matches only. British and Irish Network of. Our mission is to build healthier lives, free of cardiovascular diseases and stroke. That single purpose drives all we do. The need for our work is beyond questions. Provides guidelines, education resources etc. Http:/ www.heart.org. Antenatal Results and Choices (ARC). Http:/ www.arc-uk.org. Birth Defects Research for Children USA. Http:/ www.birthdefects.org. Http:/ www.bhf.org.uk. British Paediatric Surveillance Unit (BPSU). BPSU was joinly set ...

3

BINOCAR

http://www.binocar.org/news

Exact phrase matches only. British and Irish Network of. CARIS publishes revised table on rare diseases. To mark Rare Disease Day on February 28, CARIS has posted an updated table on genetic and syndromic rare diseases in Wales on its website. MBRRACE-UK release 'Perinatal Confidential Enquiry into Congenital Diaphragmatic Hernia' report. Results from the UK-wide confidential enquiry into the management of Congenital Diaphragmatic Hernia are released. Is 5pm Friday 5th December 2014. BINOCAR launches its...

4

BINOCAR

http://www.binocar.org/rarediseaseday

Exact phrase matches only. British and Irish Network of. CARIS publishes revised table on rare diseases. To mark Rare Disease Day. On February 28, the Congenital Anomaly Register and Information Service for Wales ( CARIS. Has posted an updated table on genetic and syndromic rare diseases in Wales on its website. The table give details of numbers reported, the prevalence and the birth ratio of these conditio. The Welsh Government recently launched the. Welsh Implementation Plan for Rare Diseases.

5

BINOCAR

http://www.binocar.org/content/Annual

Exact phrase matches only. British and Irish Network of. We are a group of. Regional and disease-specific registers collecting information about congenital anomalies occurring in the United Kingdom and the Republic of Ireland. This website provides information for health professionals, parents and other members of the public, in partnership with EUROCAT. What is a congenital anomaly? See all forthcoming events. CARIS publishes revised table on rare diseases. Website created and hosted by.

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swcar.org swcar.org

SWCAR: Frequent questions

http://www.swcar.org/swcar-faq.html

From 1 April 2015 we are part of Public Health England. We are still maintaining this website until further notice. How to notify us. Page is printer friendly. 1 What does SWCAR stand for? South West Congenital Anomaly Register. 2What is a Congenital Anomaly? 3 Do I have to ask the parents or child for consent to report the anomalies? You are not required to obtain explicit consent from parents or children. Full information on consent is given on the data protection page. 4 When should I fill in a form?

swcar.org.uk swcar.org.uk

SWCAR: Frequent questions

http://swcar.org.uk/swcar-faq.html

From 1 April 2015 we are part of Public Health England. We are still maintaining this website until further notice. How to notify us. Page is printer friendly. 1 What does SWCAR stand for? South West Congenital Anomaly Register. 2What is a Congenital Anomaly? 3 Do I have to ask the parents or child for consent to report the anomalies? You are not required to obtain explicit consent from parents or children. Full information on consent is given on the data protection page. 4 When should I fill in a form?

caris.wales.nhs.uk caris.wales.nhs.uk

Cofrestr Anomaledau Cynhenid

http://www.caris.wales.nhs.uk/hafan

Rydym yn defnyddio cwcis ar y wefan hon, a gallai fod rhai wedi cael eu gosod eisoes. Os fyddwch yn parhau i ddefnyddio'r safle heb newid eich gosodiadau, byddwn yn tybio eich bod yn cytuno â hyn. Darganfyddwch fwy am ba gwcis rydym yn eu defnyddio a pham. Asesu ymyriadau a gwasanaethau. Sut mae CARIS yn gweithio. Tablau Data and arolygon blynyddol. Datganiad ar Ansawdd Data CARIS. Hafan Iechyd Cyhoeddus Cymru. Mae'r taflen newydd CARIS wedi disodli'r adroddiad blynyddol. Sut i adrodd i CARIS. Gwefan all...

medicinesinpregnancy.org medicinesinpregnancy.org

bumps - best use of medicine in pregnancy

http://www.medicinesinpregnancy.org/Links

Cookie use on bumps. Bumps uses cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we'll assume that you are happy to receive all cookies on the Bumps website. However, if you would like to, you can change your cookie settings at any time. Best use of medicines in pregnancy. Leaflets A to Z. Leaflets A to Z. BINOCAR (British Isles Network of Congenital Anomaly Registers). ENTIS (European Network of Teratology Information Services).

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BINOCAR

Exact phrase matches only. British and Irish Network of. We are a group of researchers who work closely with several congenital anomaly registers across the United Kingdom, the Republic of Ireland and the European Union. This website, in partnership with EUROCAT,. Provides information and resources for researchers, health professionals, parents and other members of the public. What is a congenital anomaly? BINOCARD - The British and Irish Network of Congenital Anomaly Research Database.

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Binocar Data Upload Gateway

Binocar Data Upload Gateway. Enter your email address and password to access this site. Website created and hosted by.

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BINOCC - British and Irish Network of Ombudsmen and Children?s Commissioners

BINOCC - British and Irish Network of Ombudsmen and Children? For more information on the work of BINOCC please contact your Commissioner? S office using the details below:. 11 MILLION led by the Children’s Commissioner for England. 0844 800 9113 (calls charged at standard local rate 5p/minute). The Ombudsman for Children in Ireland. 52-56 Great Strand Street. LoCall 1890 654 654 or 01 865 6800. Northern Ireland Commissioner for Children and Young People. Children's Commissioner for Wales.

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