Search research articles
Contact Us
Filters
Showing results (241-250 of 310) with videos related to
Page
of 31
Sort By:
Genes
|
May 28, 2022
Independent <i>COL5A1</i> Variants in Cats with Ehlers-Danlos Syndrome
Sarah Kiener, Neoklis Apostolopoulos, Jennifer Schissler, et al.
Genes
|
October 23, 2019
Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies
Jocelyn Tanaka, Tosso Leeb, James Rushton, et al.
Briefings in Functional Genomics
|
April 1, 2010
Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses
Rebecca R Bellone, George Forsyth, Tosso Leeb, et al.
American Journal of Medical Genetics. Part A
|
February 7, 2015
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion
Elisa Tassano, Vidhya Jagannathan, Cord Drögemüller, et al.
Genes
|
May 24, 2019
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes <i>NECAP1</i> as a Novel Candidate Gene for Retinal Degeneration
Rebekkah J Hitti, James A C Oliver, Ellen C Schofield, et al.
Plos Genetics
|
May 15, 2013
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis
Katarina Tengvall, Marcin Kierczak, Kerstin Bergvall, et al.
Plos Genetics
|
December 15, 2015
Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis
Katarina Tengvall, Marcin Kierczak, Kerstin Bergvall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 6, 2023
A TNR Frameshift Variant in Weimaraner Dogs with an Exercise-Induced Paroxysmal Movement Disorder
Matthias Christen, Rodrigo Gutierrez-Quintana, Matthew James, et al.
Plos Genetics
|
March 2, 2017
A de novo variant in the ASPRV1 gene in a dog with ichthyosis
Anina Bauer, Dominik P Waluk, Arnaud Galichet, et al.
Genomics
|
November 30, 2005
Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families
June E Swinburne, Mike Boursnell, Gemma Hill, et al.
Page
of 31
Search research articles
Search
Showing results (241-250 of 310) with videos related to
Sort By:
Page
of 31
Genes
|
May 28, 2022
Independent <i>COL5A1</i> Variants in Cats with Ehlers-Danlos Syndrome
Sarah Kiener, Neoklis Apostolopoulos, Jennifer Schissler, et al.
Genes
|
October 23, 2019
Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies
Jocelyn Tanaka, Tosso Leeb, James Rushton, et al.
Briefings in Functional Genomics
|
April 1, 2010
Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses
Rebecca R Bellone, George Forsyth, Tosso Leeb, et al.
American Journal of Medical Genetics. Part A
|
February 7, 2015
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion
Elisa Tassano, Vidhya Jagannathan, Cord Drögemüller, et al.
Genes
|
May 24, 2019
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes <i>NECAP1</i> as a Novel Candidate Gene for Retinal Degeneration
Rebekkah J Hitti, James A C Oliver, Ellen C Schofield, et al.
Plos Genetics
|
May 15, 2013
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis
Katarina Tengvall, Marcin Kierczak, Kerstin Bergvall, et al.
Plos Genetics
|
December 15, 2015
Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis
Katarina Tengvall, Marcin Kierczak, Kerstin Bergvall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 6, 2023
A TNR Frameshift Variant in Weimaraner Dogs with an Exercise-Induced Paroxysmal Movement Disorder
Matthias Christen, Rodrigo Gutierrez-Quintana, Matthew James, et al.
Plos Genetics
|
March 2, 2017
A de novo variant in the ASPRV1 gene in a dog with ichthyosis
Anina Bauer, Dominik P Waluk, Arnaud Galichet, et al.
Genomics
|
November 30, 2005
Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families
June E Swinburne, Mike Boursnell, Gemma Hill, et al.
Page
of 31