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Results of search for 'au:"Stambolian, D E"'
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Authors
Borns, P
Bragin, A
Cardonick, E
Chepelinsky, A B
Deen, P M
Favor, J
Grimes, P A
Kronwith, S D
LaRossa, D
Lu, Y
McDonald, D M
Neuhäuser-Klaus, A
Ohtaka-Maruyama, C
Onyx, P
Parker-Wilson, D M
Pretsch, W
Quinn, G
Sidjanin, D J
Skach, W R
Stambolian, D E
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Topics
Adolescent
Animals
Animals, Newborn
Aquaporins
Blotting, Western
Cataract
Cell Line
Child
Chromosome Mapping
Chromosomes
Cleft Palate
Female
Humans
Lens, Crystalline
Male
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Mutation
genetics
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English
Your search returned 3 results.
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1.
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16.
[electronic resource]
by
Sidjanin, D J
Grimes, P A
Pretsch, W
Neuhäuser-Klaus, A
Favor, J
Stambolian, D E
Producer:
19971204
In:
Investigative ophthalmology & visual science
vol. 38
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No items available.
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2.
Stickler's syndrome in the Cleft Palate Clinic.
[electronic resource]
by
Kronwith, S D
Quinn, G
McDonald, D M
Cardonick, E
Onyx, P
LaRossa, D
Borns, P
Stambolian, D E
Zackai, E H
Producer:
19910108
In:
Journal of pediatric ophthalmology and strabismus
vol. 27
Online resources:
Available from publisher's website
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No items available.
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3.
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice.
[electronic resource]
by
Sidjanin, D J
Parker-Wilson, D M
Neuhäuser-Klaus, A
Pretsch, W
Favor, J
Deen, P M
Ohtaka-Maruyama, C
Lu, Y
Bragin, A
Skach, W R
Chepelinsky, A B
Grimes, P A
Stambolian, D E
Producer:
20010913
In:
Genomics
vol. 74
Online resources:
Available from publisher's website
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No items available.
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