Molecular neonatal screening for homocystinuria in the Qatari population-Reference-Cited by-同舟云学术

Molecular neonatal screening for homocystinuria in the Qatari population

Published:2009-06 Issue:6 Volume:30 Page:1021-1022
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Zschocke Johannes,Kebbewar Moustafa,Gan-Schreier Hongying,Fischer Christine,Fang-Hoffmann Junmin,Wilrich Julia,Abdoh Ghassan,Ben-Omran Tawfeg,Shahbek Noora,Lindner Martin,Al Rifai Hilal,Al Khal Abdul Latif,Hoffmann Georg F.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference6 articles.

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2. Neonatal screening: from the ‘Guthrie age’ to the ‘genetic age’;Dhondt;J Inherit Metab Dis,2007

3. A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population;El-Said;Hum Mutat,2006

4. Expanded newborn screening for biochemical disorders: the effect of a false-positive result;Gurian;Pediatrics,2006

5. Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis;Ranieri;BMJ,1991

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