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C R Marshall

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Cytogenetic and Genome Research|March 17, 2009

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.

Biology Letters|September 7, 2018

Quantifying the dark data in museum fossil collections as palaeontology undergoes a second digital revolutionC R Marshall, S Finnegan, E C Clites, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001

Effects of sampling standardization on estimates of Phanerozoic marine diversificationJ Alroy, C R Marshall, R K Bambach, et al.

Clinical Genetics|August 19, 2014

Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Cytogenetic and Genome Research|March 17, 2009

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.

Biology Letters|September 7, 2018

Quantifying the dark data in museum fossil collections as palaeontology undergoes a second digital revolutionC R Marshall, S Finnegan, E C Clites, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001

Effects of sampling standardization on estimates of Phanerozoic marine diversificationJ Alroy, C R Marshall, R K Bambach, et al.

Clinical Genetics|August 19, 2014

Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.

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