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M H Breuning

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European Journal of Medical Genetics|March 25, 2009

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.

Journal of Medical Genetics|September 6, 2005

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)M Nielsen, P F Franken, T H C M Reinards, et al.

The Journal of Clinical Endocrinology and Metabolism|October 11, 2013

The IGSF1 deficiency syndrome: characteristics of male and female patientsS D Joustra, N Schoenmakers, L Persani, et al.

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Search research articles

Showing results (161-170 of 163) with videos related to

Sort By:

Pageof 17

You have reached the last page of results.This site can display upto 163 results.

European Journal of Medical Genetics|March 25, 2009

Journal of Medical Genetics|September 6, 2005

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)M Nielsen, P F Franken, T H C M Reinards, et al.

The Journal of Clinical Endocrinology and Metabolism|October 11, 2013

The IGSF1 deficiency syndrome: characteristics of male and female patientsS D Joustra, N Schoenmakers, L Persani, et al.

Pageof 17