W T Brown|J C Bauer - JoVE Visualize

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JMIR Formative Research|August 18, 2025

Optimizing the Postcataract Patient Journey Using AI-Driven Teleconsultation: Prospective Case StudyJoukje C Wanten, Noël J C Bauer, Mohita Chowdhury, et al.

Clinical Genetics|June 25, 2010

Autism severity is associated with child and maternal MAOA genotypesI L Cohen, X Liu, M E S Lewis, et al.

Experimental Neurology|June 1, 1990

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.

American Journal of Medical Genetics|February 1, 1991

Fragile X screening program in New York StateS L Nolin, D A Snider, E C Jenkins, et al.

Neurology|March 1, 1991

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.

Lancet (London, England)|September 18, 1993

Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseasesA M Saunders, K Schmader, J C Breitner, et al.

Experimental Neurology|November 1, 1989

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeD Goldgaber, L G Goldfarb, P Brown, et al.

American Journal of Medical Genetics|July 15, 1994

Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptusesS L Sherman, A Maddalena, P N Howard-Peebles, et al.

Molecular Genetics and Metabolism|June 5, 1999

Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 geneJ M Hartikainen, W Ju, K E Wisniewski, et al.

American Journal of Medical Genetics|April 1, 1992

Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndromeV J Hinton, C S Dobkin, J M Halperin, et al.

Pageof 23

Showing results (181-190 of 227) with videos related to

Sort By:

Pageof 23

JMIR Formative Research|August 18, 2025

Optimizing the Postcataract Patient Journey Using AI-Driven Teleconsultation: Prospective Case StudyJoukje C Wanten, Noël J C Bauer, Mohita Chowdhury, et al.

Clinical Genetics|June 25, 2010

Autism severity is associated with child and maternal MAOA genotypesI L Cohen, X Liu, M E S Lewis, et al.

Experimental Neurology|June 1, 1990

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.

American Journal of Medical Genetics|February 1, 1991

Fragile X screening program in New York StateS L Nolin, D A Snider, E C Jenkins, et al.

Neurology|March 1, 1991

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.

Lancet (London, England)|September 18, 1993

Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseasesA M Saunders, K Schmader, J C Breitner, et al.

Experimental Neurology|November 1, 1989

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeD Goldgaber, L G Goldfarb, P Brown, et al.

American Journal of Medical Genetics|July 15, 1994

Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptusesS L Sherman, A Maddalena, P N Howard-Peebles, et al.

Molecular Genetics and Metabolism|June 5, 1999

Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 geneJ M Hartikainen, W Ju, K E Wisniewski, et al.

American Journal of Medical Genetics|April 1, 1992

Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndromeV J Hinton, C S Dobkin, J M Halperin, et al.

Pageof 23