Modell, Bernadette
Bernadette Modell
موديل، برناديت
Modell, Bernadette 1931-....
Modell, B.
VIAF ID: 9919755 (Personal)
Permalink: http://viaf.org/viaf/9919755
Preferred Forms
- 100 0 _ ‡a Bernadette Modell
- 200 _ | ‡a Modell ‡b Bernadette ‡f 1931-....
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- 100 1 _ ‡a Modell, Bernadette
- 100 1 _ ‡a Modell, Bernadette
- 100 1 _ ‡a Modell, Bernadette
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- 100 1 _ ‡a Modell, Bernadette
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4xx's: Alternate Name Forms (13)
Works
Title | Sources |
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The changing epidemiology of β-thalassemia in the Greek-Cypriot population | |
The clinical approach to ... 1984 | |
Collecting genetic information in primary care: evaluating a new family history tool | |
Community genetics services in Europe : report on a survey | |
Congenital disorders: epidemiological methods for answering calls for action | |
A different molecular pattern of beta-thalassemia mutations in northeast Brazil | |
DTPA in the management of iron overload in thalassaemia | |
Estimates of global and regional prevalence of neural tube defects for 2015: a systematic analysis. | |
Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives | |
Folic acid to reduce neonatal mortality from neural tube disorders | |
From DNA to the community : International Conference on Community genetics, June 20-22, 2000, Jonquière (Québec) | |
Global epidemiology of haemoglobin disorders and derived service indicators | |
GPs' opinions of their role in prenatal genetic services: a cross-sectional survey | |
Improved survival of thalassaemia major in the UK and relation to T2* cardiovascular magnetic resonance | |
Informing carriers of beta-thalassemia: giving the good news. | |
Iranian national thalassaemia screening programme | |
Medical genetics in developing countries | |
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders | |
The Olivieri case | |
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide | |
Science and society: genetic counselling and customary consanguineous marriage | |
services génétiques au sein de la collectivité en Europe rapport sur une enquête | |
Sickle-cell disorders: limits of descriptive epidemiology | |
Socio-economic inequalities as a predictor of health in South Africa--the Yenza cross-sectional study | |
Systematic Review and Meta-Analysis of the Birth Prevalence of Orofacial Clefts in Low- and Middle-Income Countries | |
Timeline: Raising the profile of genetics in primary care | |
Towards a healthy baby, 1992: | |
Transfusion-dependent thalassaemia: a new era. | |
What is thalassaemia. | |
ما هي الثلاسيميا؟ : فقر دم (أنيميا) البحر الابيض المتوسط (فقر الدم الوراثي) |