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1.

Serpentine fibula and neurofibromatosis type 1: a rare association.
by Atalar, H

Acta paediatrica (Oslo, Norway : 1992), March 2011, Vol.100(3), pp.318-319

4.

Single nucleotide polymorphisms predict symptom severity of autism spectrum disorder.
by Jiao, Yun

Journal of autism and developmental disorders, June 2012, Vol.42(6), pp.971-983

6.

Brief report: MECP2 mutations in people without Rett syndrome.
by Suter, Bernhard

Journal of autism and developmental disorders, March 2014, Vol.44(3), pp.703-711

10.

Father's genetic quest pays off.
by Maher, Brendan

Nature, June 27, 2013, Vol.498(7455), pp.418-419

20.

Family history of premature death and risk of early onset cardiovascular disease.
by Ranthe, Mattis Flyvholm

Journal of the American College of Cardiology, August 28, 2012, Vol.60(9), pp.814-821

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