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H M Hittner

Showing results (31-40 of 58) with videos related to

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American Journal of Human Genetics|January 1, 1983
Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locusR E Ferrell, H M Hittner, J H Antoszyk
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1981
Ocular manifestations of the Smith-Lemli-Opitz syndromeF L Kretzer, H M Hittner, R S Mehta
American Journal of Human Genetics|November 1, 1982
Linkage studies in carriers of Lowe oculo-cerebro-renal syndromeH M Hittner, A J Carroll, J T Prchal
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1980
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2R E Ferrell, A Chakravarti, H M Hittner, et al.
The British Journal of Ophthalmology|March 1, 1984
Atypical vitelliform macular dystrophy in a 5-generation familyH M Hittner, R E Ferrell, R P Borda, et al.
American Journal of Medical Genetics|January 1, 1980
Duplication 11p11.3 leads to 14.1 to meiotic crossing--overR J Strobel, V M Riccardi, D H Ledbetter, et al.
American Journal of Human Genetics|March 1, 1982
Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4R E Ferrell, H M Hittner, F L Kretzer, et al.
Bulletin of the New York Academy of Medicine|December 1, 1985
Pathogenic mechanism of retinopathy of prematurity: a controversial explanation for the efficacy of oral and intramuscular vitamin E supplementation and cryotherapyF L Kretzer, A R McPherson, A J Rudolph, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 1, 1979
Colobomatous microphthalmia, heart disease, hearing loss, and mental retardation--a syndromeH M Hittner, N J Hirsch, G M Kreh, et al.
American Journal of Ophthalmology|April 1, 1980
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteriaH M Hittner, V M Riccardi, R E Ferrell, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|January 1, 1983
Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locusR E Ferrell, H M Hittner, J H Antoszyk
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1981
Ocular manifestations of the Smith-Lemli-Opitz syndromeF L Kretzer, H M Hittner, R S Mehta
American Journal of Human Genetics|November 1, 1982
Linkage studies in carriers of Lowe oculo-cerebro-renal syndromeH M Hittner, A J Carroll, J T Prchal
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1980
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2R E Ferrell, A Chakravarti, H M Hittner, et al.
The British Journal of Ophthalmology|March 1, 1984
Atypical vitelliform macular dystrophy in a 5-generation familyH M Hittner, R E Ferrell, R P Borda, et al.
American Journal of Medical Genetics|January 1, 1980
Duplication 11p11.3 leads to 14.1 to meiotic crossing--overR J Strobel, V M Riccardi, D H Ledbetter, et al.
American Journal of Human Genetics|March 1, 1982
Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4R E Ferrell, H M Hittner, F L Kretzer, et al.
Bulletin of the New York Academy of Medicine|December 1, 1985
Pathogenic mechanism of retinopathy of prematurity: a controversial explanation for the efficacy of oral and intramuscular vitamin E supplementation and cryotherapyF L Kretzer, A R McPherson, A J Rudolph, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 1, 1979
Colobomatous microphthalmia, heart disease, hearing loss, and mental retardation--a syndromeH M Hittner, N J Hirsch, G M Kreh, et al.
American Journal of Ophthalmology|April 1, 1980
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteriaH M Hittner, V M Riccardi, R E Ferrell, et al.
Pageof 6