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M Mancini

Showing results (791-800 of 794) with videos related to

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European Journal of Human Genetics : EJHG|June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genesAimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Cancer Research|March 9, 2005
Large-scale transcriptome analyses reveal new genetic marker candidates of head, neck, and thyroid cancerEduardo M Reis, Elida P B Ojopi, Fernando L Alberto, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability SyndromeJung-Hyun Kim, Deepali N Shinde, Margot R F Reijnders, et al.
Pageof 80

Showing results (791-800 of 794) with videos related to

Sort By:
Pageof 80
You have reached the last page of results.This site can display upto 794 results.
European Journal of Human Genetics : EJHG|June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genesAimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Cancer Research|March 9, 2005
Large-scale transcriptome analyses reveal new genetic marker candidates of head, neck, and thyroid cancerEduardo M Reis, Elida P B Ojopi, Fernando L Alberto, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability SyndromeJung-Hyun Kim, Deepali N Shinde, Margot R F Reijnders, et al.
Pageof 80