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R M Liberfarb

Showing results (11-20 of 23) with videos related to

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Annals of Ophthalmology|June 1, 1987
Ocular coloboma associated with a solitary maxillary central incisor and growth failure: manifestations of holoprosencephalyR M Liberfarb, O P Abdo, R C Pruett
American Journal of Ophthalmology|November 1, 1979
Hereditary progressive arthro-ophthalmopathy of SticklerN P Blair, D M Albert, R M Liberfarb, et al.
American Journal of Medical Genetics|January 1, 1979
Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two familiesR M Liberfarb, W R Breg, L Atkins, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1986
Tapetoretinal degeneration associated with multisystem abnormalities. A case reportR M Liberfarb, O Katsumi, E Fleischnick, et al.
American Journal of Ophthalmology|August 15, 1990
Distinctive cataract in the Stickler syndromeC M Seery, R C Pruett, R M Liberfarb, et al.
Journal of Child Neurology|July 1, 1993
Unique hereditary sensory and autonomic neuropathy with growth hormone deficiencyR M Liberfarb, A H Jackson, R D Eavey, et al.
American Journal of Otolaryngology|March 1, 1990
Histopathology of the ears, eyes, and brain in Norrie's disease (oculoacousticocerebral degeneration)J B Nadol, R D Eavey, R M Liberfarb, et al.
Ophthalmology|October 1, 1985
Norrie's disease: a study of two familiesR M Liberfarb, R D Eavey, G R De Long, et al.
Genomics|December 1, 1987
The Stickler syndrome: evidence for close linkage to the structural gene for type II collagenC A Francomano, R M Liberfarb, T Hirose, et al.
Pathology and Immunopathology Research|January 1, 1988
The Stickler syndrome is closely linked to COL2A1, the structural gene for type II collagenC A Francomano, R M Liberfarb, T Hirose, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Annals of Ophthalmology|June 1, 1987
Ocular coloboma associated with a solitary maxillary central incisor and growth failure: manifestations of holoprosencephalyR M Liberfarb, O P Abdo, R C Pruett
American Journal of Ophthalmology|November 1, 1979
Hereditary progressive arthro-ophthalmopathy of SticklerN P Blair, D M Albert, R M Liberfarb, et al.
American Journal of Medical Genetics|January 1, 1979
Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two familiesR M Liberfarb, W R Breg, L Atkins, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1986
Tapetoretinal degeneration associated with multisystem abnormalities. A case reportR M Liberfarb, O Katsumi, E Fleischnick, et al.
American Journal of Ophthalmology|August 15, 1990
Distinctive cataract in the Stickler syndromeC M Seery, R C Pruett, R M Liberfarb, et al.
Journal of Child Neurology|July 1, 1993
Unique hereditary sensory and autonomic neuropathy with growth hormone deficiencyR M Liberfarb, A H Jackson, R D Eavey, et al.
American Journal of Otolaryngology|March 1, 1990
Histopathology of the ears, eyes, and brain in Norrie's disease (oculoacousticocerebral degeneration)J B Nadol, R D Eavey, R M Liberfarb, et al.
Ophthalmology|October 1, 1985
Norrie's disease: a study of two familiesR M Liberfarb, R D Eavey, G R De Long, et al.
Genomics|December 1, 1987
The Stickler syndrome: evidence for close linkage to the structural gene for type II collagenC A Francomano, R M Liberfarb, T Hirose, et al.
Pathology and Immunopathology Research|January 1, 1988
The Stickler syndrome is closely linked to COL2A1, the structural gene for type II collagenC A Francomano, R M Liberfarb, T Hirose, et al.
Pageof 3