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Alex Levin

Showing results (11-20 of 18) with videos related to

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Clinical Biochemistry|September 23, 2010
Pediatric reference intervals for lymphocyte vitamin C (ascorbic acid)Alex Levin, Charmaine DeSouza, Christian Zaarour, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2006
Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndromeAnuradha Ganesh, Charles Smith, Wilson Chan, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
Ophthalmic Genetics|July 18, 2003
Mutational analysis of the OA1 gene in ocular albinismOlivier Camand, Sandrine Boutboul, Laurence Arbogast, et al.
Minnesota Medicine|March 3, 2010
Evidence outweighs beliefRandell Alexander, Ronald G Barr, Robert Block, et al.
American Journal of Medical Genetics|February 22, 2002
Apparent genotype-phenotype correlation in childhood, adolescent, and adult Chediak-Higashi syndromeMohammad A Karim, Koji Suzuki, Kazuyoshi Fukai, et al.
Orphanet Journal of Rare Diseases|March 11, 2026
Recommendations for the diagnosis and management of cln3 disease (batten disease) using the Delphi consensus methodologyJonathan W Mink, Heather R Adams, Rebecca Ahrens-Nicklas, et al.
Human Mutation|April 13, 2021
CNGB1-related rod-cone dystrophy: A mutation review and updateMarco Nassisi, Vasily M Smirnov, Cyntia Solis Hernandez, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Clinical Biochemistry|September 23, 2010
Pediatric reference intervals for lymphocyte vitamin C (ascorbic acid)Alex Levin, Charmaine DeSouza, Christian Zaarour, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2006
Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndromeAnuradha Ganesh, Charles Smith, Wilson Chan, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
Ophthalmic Genetics|July 18, 2003
Mutational analysis of the OA1 gene in ocular albinismOlivier Camand, Sandrine Boutboul, Laurence Arbogast, et al.
Minnesota Medicine|March 3, 2010
Evidence outweighs beliefRandell Alexander, Ronald G Barr, Robert Block, et al.
American Journal of Medical Genetics|February 22, 2002
Apparent genotype-phenotype correlation in childhood, adolescent, and adult Chediak-Higashi syndromeMohammad A Karim, Koji Suzuki, Kazuyoshi Fukai, et al.
Orphanet Journal of Rare Diseases|March 11, 2026
Recommendations for the diagnosis and management of cln3 disease (batten disease) using the Delphi consensus methodologyJonathan W Mink, Heather R Adams, Rebecca Ahrens-Nicklas, et al.
Human Mutation|April 13, 2021
CNGB1-related rod-cone dystrophy: A mutation review and updateMarco Nassisi, Vasily M Smirnov, Cyntia Solis Hernandez, et al.
Pageof 2