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P B Mullaney

Showing results (31-40 of 34) with videos related to

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Ophthalmology|April 17, 1998
Keratoconjunctivitis sicca associated with achalasia of the cardia, adrenocortical insufficiency, and lacrimal gland degeneration: Keratoconjunctivitis sicca secondary to lacrimal gland degeneration may parallel degenerative changes in esophageal and adrenocortical functionP B Mullaney, R Weatherhead, L Millar, et al.
American Journal of Human Genetics|July 31, 1998
Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13S M Wang, J Zwaan, P B Mullaney, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 10, 2000
Recognized globe perforation during strabismus surgery: incidence, risk factors, and sequelaeA H Awad, P B Mullaney, A Al-Hazmi, et al.
Nature Genetics|October 16, 2001
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2M Nakano, K Yamada, J Fain, et al.
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Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Ophthalmology|April 17, 1998
Keratoconjunctivitis sicca associated with achalasia of the cardia, adrenocortical insufficiency, and lacrimal gland degeneration: Keratoconjunctivitis sicca secondary to lacrimal gland degeneration may parallel degenerative changes in esophageal and adrenocortical functionP B Mullaney, R Weatherhead, L Millar, et al.
American Journal of Human Genetics|July 31, 1998
Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13S M Wang, J Zwaan, P B Mullaney, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 10, 2000
Recognized globe perforation during strabismus surgery: incidence, risk factors, and sequelaeA H Awad, P B Mullaney, A Al-Hazmi, et al.
Nature Genetics|October 16, 2001
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2M Nakano, K Yamada, J Fain, et al.
Pageof 4