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Journal of Medical Genetics
|
August 4, 2010
Critical consequences of finding three pathogenic mutations in an individual with recessive disease
Sally Halsall, Adeline K Nicholas, Gemma Thornton, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2023
Ophthalmic manifestations of Czech dysplasia
Zack Soh, Howard Martin, Allan J Richards, et al.
Journal of the American Veterinary Medical Association
|
September 1, 1986
Clostridium perfringens type C enterotoxemia in a newborn foal
M Howard-Martin, R J Morton, C W Qualls, et al.
Biochemical Pharmacology
|
May 13, 2022
Spatial analysis of drug absorption, distribution, metabolism, and toxicology using mass spectrometry imaging
Michelle L Spruill, Mirjana Maletic-Savatic, Howard Martin, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2016
Molecularly proven mosaicism in phenotypically normal parent of a girl with Freeman-Sheldon Syndrome caused by a pathogenic MYH3 mutation
Jennifer Hague, Isabelle Delon, Kim Brugger, et al.
Genes
|
June 24, 2022
Dominant Stickler Syndrome
Zack Soh, Allan J Richards, Annie McNinch, et al.
Genes
|
July 27, 2022
Autosomal Recessive Stickler Syndrome
Thomas R W Nixon, Allan J Richards, Howard Martin, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 16, 2025
Myopia progression in children with Stickler syndrome: a longitudinal cohort study
Nisha Nixon, Kelly H Cheng, Allan Richards, et al.
Progress in Retinal and Eye Research
|
September 30, 2024
Pathobiology of the crystalline lens in Stickler syndrome
Martin P Snead, Frank J Lovicu, Thomas Rw Nixon, et al.
BMC Nephrology
|
June 3, 2014
Unilateral hypoplastic kidney - a novel highly penetrant feature of familial juvenile hyperuricaemic nephropathy
Lucy A Plumb, Matko Marlais, Agnieszka Bierzynska, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
Journal of Medical Genetics
|
August 4, 2010
Critical consequences of finding three pathogenic mutations in an individual with recessive disease
Sally Halsall, Adeline K Nicholas, Gemma Thornton, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2023
Ophthalmic manifestations of Czech dysplasia
Zack Soh, Howard Martin, Allan J Richards, et al.
Journal of the American Veterinary Medical Association
|
September 1, 1986
Clostridium perfringens type C enterotoxemia in a newborn foal
M Howard-Martin, R J Morton, C W Qualls, et al.
Biochemical Pharmacology
|
May 13, 2022
Spatial analysis of drug absorption, distribution, metabolism, and toxicology using mass spectrometry imaging
Michelle L Spruill, Mirjana Maletic-Savatic, Howard Martin, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2016
Molecularly proven mosaicism in phenotypically normal parent of a girl with Freeman-Sheldon Syndrome caused by a pathogenic MYH3 mutation
Jennifer Hague, Isabelle Delon, Kim Brugger, et al.
Genes
|
June 24, 2022
Dominant Stickler Syndrome
Zack Soh, Allan J Richards, Annie McNinch, et al.
Genes
|
July 27, 2022
Autosomal Recessive Stickler Syndrome
Thomas R W Nixon, Allan J Richards, Howard Martin, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 16, 2025
Myopia progression in children with Stickler syndrome: a longitudinal cohort study
Nisha Nixon, Kelly H Cheng, Allan Richards, et al.
Progress in Retinal and Eye Research
|
September 30, 2024
Pathobiology of the crystalline lens in Stickler syndrome
Martin P Snead, Frank J Lovicu, Thomas Rw Nixon, et al.
BMC Nephrology
|
June 3, 2014
Unilateral hypoplastic kidney - a novel highly penetrant feature of familial juvenile hyperuricaemic nephropathy
Lucy A Plumb, Matko Marlais, Agnieszka Bierzynska, et al.
Page
of 4