Volume 34 Number 22 June 4-11, 2015
Birth Defects and Child Health
A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field.
El Malti R et al. Eur. J. Hum. Genet. 2015 May 27.
El Malti R et al. Eur. J. Hum. Genet. 2015 May 27.
A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.
Noke M et al. Eur. J. Hum. Genet. 2015 May 27.
Noke M et al. Eur. J. Hum. Genet. 2015 May 27.
Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries.
Zerjav TM et al. Orphanet J Rare Dis 2015 10(1) 68
Zerjav TM et al. Orphanet J Rare Dis 2015 10(1) 68
The Swiss National Registry for Primary Immunodeficiencies: Report on the first 6 years' activity 2008-2014.
Marschall K et al. Clin. Exp. Immunol. 2015 Jun 1.
Marschall K et al. Clin. Exp. Immunol. 2015 Jun 1.
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