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Neurology|September 23, 2009

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.

Cell Death Discovery|June 9, 2016

Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.

Clinical Genetics|September 17, 2013

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmiaN Chassaing, A Causse, A Vigouroux, et al.

Revue Neurologique|August 20, 2013

[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.

Pageof 7

Search research articles

Showing results (61-70 of 64) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 64 results.

Neurology|September 23, 2009

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.

Cell Death Discovery|June 9, 2016

Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.

Clinical Genetics|September 17, 2013

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmiaN Chassaing, A Causse, A Vigouroux, et al.

Revue Neurologique|August 20, 2013

[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.

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