C R Marshall|F M Maynard - JoVE Visualize

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Systematic Biology|April 27, 2002

Molecular systematics of the CanidaeR K Wayne, E Geffen, D J Girman, et al.

Oncogene|March 23, 1999

Mutations of c-kit JM domain are found in a minority of human gastrointestinal stromal tumorsC A Moskaluk, Q Tian, C R Marshall, et al.

Research in Developmental Disabilities|September 25, 2016

Narrative skills in deaf children who use spoken English: Dissociations between macro and microstructural devices-A C Jones, E Toscano, N Botting, et al.

Clinical Genetics|March 30, 2010

Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.

Clinical Genetics|November 23, 2016

Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.

Clinical Genetics|December 1, 2010

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.

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

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 40 results.

Systematic Biology|April 27, 2002

Molecular systematics of the CanidaeR K Wayne, E Geffen, D J Girman, et al.

Oncogene|March 23, 1999

Mutations of c-kit JM domain are found in a minority of human gastrointestinal stromal tumorsC A Moskaluk, Q Tian, C R Marshall, et al.

Research in Developmental Disabilities|September 25, 2016

Narrative skills in deaf children who use spoken English: Dissociations between macro and microstructural devices-A C Jones, E Toscano, N Botting, et al.

Clinical Genetics|March 30, 2010

Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.

Clinical Genetics|November 23, 2016

Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.

Clinical Genetics|December 1, 2010

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.

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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