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1-4 of 4 results for MCPH1

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Open accessResearch articleFirst published January, 2014

A High-Throughput Assay to Identify Modifiers of Premature Chromosome Condensation

Matthew Adams, Victoria J. Cookson, Julie Higgins [...]

Journal of Biomolecular Screening

Restricted accessResearch articleFirst published July, 2016

The Impact of rs3762271 and rs930557 Polymorphisms of ASPM and MCPH1 Genes on the Anatomy and Function of the Brain

Joanna Pierzak-Sominka, Karolina Skonieczna-Żydecka, Jacek Rudnicki [...]

Biological Research For Nursing

Restricted accessResearch articleFirst published June, 2008

Genes,Brains,and Language: An Epistemological Examination of how Genes can Underlie Human Cognitive Behavior

Nathalie Gontier

Review of General Psychology

Restricted accessResearch articleFirst published January, 2021

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment

Oluwafemi G Oluwole, Kevin K Esoh, Edmond Wonkam-Tingang [...]

Experimental Biology and Medicine

Search results

Articles (4)

Journals (0)

1-4 of 4 results for MCPH1

Sort by:

Relevance

Select all

Sort by:

Relevance

Open accessResearch articleFirst published January, 2014

A High-Throughput Assay to Identify Modifiers of Premature Chromosome Condensation

Matthew Adams, Victoria J. Cookson, Julie Higgins [...]

Journal of Biomolecular Screening

Restricted accessResearch articleFirst published July, 2016

The Impact of rs3762271 and rs930557 Polymorphisms of ASPM and MCPH1 Genes on the Anatomy and Function of the Brain

Joanna Pierzak-Sominka, Karolina Skonieczna-Żydecka, Jacek Rudnicki [...]

Biological Research For Nursing

Restricted accessResearch articleFirst published June, 2008

Genes,Brains,and Language: An Epistemological Examination of how Genes can Underlie Human Cognitive Behavior

Nathalie Gontier

Review of General Psychology

Restricted accessResearch articleFirst published January, 2021

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment

Oluwafemi G Oluwole, Kevin K Esoh, Edmond Wonkam-Tingang [...]

Experimental Biology and Medicine