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481.
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Patient delay in seeking care for heart attack symptoms: findings from focus groups conducted in five U.S. regions. [electronic resource] by
- Finnegan, J R
- Meischke, H
- Zapka, J G
- Leviton, L
- Meshack, A
- Benjamin-Garner, R
- Estabrook, B
- Hall, N J
- Schaeffer, S
- Smith, C
- Weitzman, E R
- Raczynski, J
- Stone, E
Producer: 20001006
In:
Preventive medicine vol. 31
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482.
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A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye. [electronic resource] by
- Nishimura, D Y
- Searby, C C
- Alward, W L
- Walton, D
- Craig, J E
- Mackey, D A
- Kawase, K
- Kanis, A B
- Patil, S R
- Stone, E M
- Sheffield, V C
Producer: 20010308
In:
American journal of human genetics vol. 68
Availability: No items available.
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483.
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Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A) [electronic resource] by
- Alward, W L
- Fingert, J H
- Coote, M A
- Johnson, A T
- Lerner, S F
- Junqua, D
- Durcan, F J
- McCartney, P J
- Mackey, D A
- Sheffield, V C
- Stone, E M
Producer: 19980409
In:
The New England journal of medicine vol. 338
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484.
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School physical education: effect of the Child and Adolescent Trial for Cardiovascular Health. [electronic resource] by
- McKenzie, T L
- Nader, P R
- Strikmiller, P K
- Yang, M
- Stone, E J
- Perry, C L
- Taylor, W C
- Epping, J N
- Feldman, H A
- Luepker, R V
- Kelder, S H
Producer: 19961105
In:
Preventive medicine vol. 25
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485.
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Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier. [electronic resource] by
- Craig, J E
- Baird, P N
- Healey, D L
- McNaught, A I
- McCartney, P J
- Rait, J L
- Dickinson, J L
- Roe, L
- Fingert, J H
- Stone, E M
- Mackey, D A
Producer: 20010920
In:
Ophthalmology vol. 108
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486.
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Mutations in the SMAD4/DPC4 gene in juvenile polyposis. [electronic resource] by
- Howe, J R
- Roth, S
- Ringold, J C
- Summers, R W
- Järvinen, H J
- Sistonen, P
- Tomlinson, I P
- Houlston, R S
- Bevan, S
- Mitros, F A
- Stone, E M
- Aaltonen, L A
Producer: 19980604
In:
Science (New York, N.Y.) vol. 280
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487.
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Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa. [electronic resource] by
- Jacobson, S G
- Cideciyan, A V
- Iannaccone, A
- Weleber, R G
- Fishman, G A
- Maguire, A M
- Affatigato, L M
- Bennett, J
- Pierce, E A
- Danciger, M
- Farber, D B
- Stone, E M
Producer: 20000614
In:
Investigative ophthalmology & visual science vol. 41
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488.
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Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. [electronic resource] by
- Swain, P K
- Chen, S
- Wang, Q L
- Affatigato, L M
- Coats, C L
- Brady, K D
- Fishman, G A
- Jacobson, S G
- Swaroop, A
- Stone, E
- Sieving, P A
- Zack, D J
Producer: 19980129
In:
Neuron vol. 19
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489.
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CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype. [electronic resource] by
- Burnight, E R
- Wiley, L A
- Drack, A V
- Braun, T A
- Anfinson, K R
- Kaalberg, E E
- Halder, J A
- Affatigato, L M
- Mullins, R F
- Stone, E M
- Tucker, B A
Producer: 20150219
In:
Gene therapy vol. 21
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490.
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Changes in nutrient intakes of elementary school children following a school-based intervention: results from the CATCH Study. [electronic resource] by
- Lytle, L A
- Stone, E J
- Nichaman, M Z
- Perry, C L
- Montgomery, D H
- Nicklas, T A
- Zive, M M
- Mitchell, P
- Dwyer, J T
- Ebzery, M K
- Evans, M A
- Galati, T P
Producer: 19961105
In:
Preventive medicine vol. 25
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491.
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Observation of the ⁶⁰Fe nucleosynthesis-clock isotope in galactic cosmic rays. [electronic resource] by
- Binns, W R
- Israel, M H
- Christian, E R
- Cummings, A C
- de Nolfo, G A
- Lave, K A
- Leske, R A
- Mewaldt, R A
- Stone, E C
- von Rosenvinge, T T
- Wiedenbeck, M E
Producer: 20160607
In:
Science (New York, N.Y.) vol. 352
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492.
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Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21. [electronic resource] by
- Héon, E
- Piguet, B
- Munier, F
- Sneed, S R
- Morgan, C M
- Forni, S
- Pescia, G
- Schorderet, D
- Taylor, C M
- Streb, L M
- Wiles, C D
- Nishimura, D Y
- Sheffield, V C
- Stone, E M
Producer: 19960304
In:
Archives of ophthalmology (Chicago, Ill. : 1960) vol. 114
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493.
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Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor. [electronic resource] by
- Jacobson, N
- Andrews, M
- Shepard, A R
- Nishimura, D
- Searby, C
- Fingert, J H
- Hageman, G
- Mullins, R
- Davidson, B L
- Kwon, Y H
- Alward, W L
- Stone, E M
- Clark, A F
- Sheffield, V C
Producer: 20010315
In:
Human molecular genetics vol. 10
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494.
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Mutations in the CRB1 gene cause Leber congenital amaurosis. [electronic resource] by
- Lotery, A J
- Jacobson, S G
- Fishman, G A
- Weleber, R G
- Fulton, A B
- Namperumalsamy, P
- Héon, E
- Levin, A V
- Grover, S
- Rosenow, J R
- Kopp, K K
- Sheffield, V C
- Stone, E M
Producer: 20010405
In:
Archives of ophthalmology (Chicago, Ill. : 1960) vol. 119
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495.
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Human uteroglobin gene: structure, subchromosomal localization, and polymorphism. [electronic resource] by
- Zhang, Z
- Zimonjic, D B
- Popescu, N C
- Wang, N
- Gerhard, D S
- Stone, E M
- Arbour, N C
- De Vries, H G
- Scheffer, H
- Gerritsen, J
- Colle'e, J M
- Ten Kate, L P
- Mukherjee, A B
Producer: 19970227
In:
DNA and cell biology vol. 16
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496.
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Changes in the nutrient content of school lunches: results from the CATCH Eat Smart Food service Intervention. [electronic resource] by
- Osganian, S K
- Ebzery, M K
- Montgomery, D H
- Nicklas, T A
- Evans, M A
- Mitchell, P D
- Lytle, L A
- Snyder, M P
- Stone, E J
- Zive, M M
- Bachman, K J
- Rice, R
- Parcel, G S
Producer: 19961105
In:
Preventive medicine vol. 25
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497.
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Three-year maintenance of improved diet and physical activity: the CATCH cohort. Child and Adolescent Trial for Cardiovascular Health. [electronic resource] by
- Nader, P R
- Stone, E J
- Lytle, L A
- Perry, C L
- Osganian, S K
- Kelder, S
- Webber, L S
- Elder, J P
- Montgomery, D
- Feldman, H A
- Wu, M
- Johnson, C
- Parcel, G S
- Luepker, R V
Producer: 19990803
In:
Archives of pediatrics & adolescent medicine vol. 153
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498.
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Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head. [electronic resource] by
- Clark, A F
- Kawase, K
- English-Wright, S
- Lane, D
- Steely, H T
- Yamamoto, T
- Kitazawa, Y
- Kwon, Y H
- Fingert, J H
- Swiderski, R E
- Mullins, R F
- Hageman, G S
- Alward, W L
- Sheffield, V C
- Stone, E M
Producer: 20010614
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 15
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499.
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An analysis of allelic variation in the ABCA4 gene. [electronic resource] by
- Webster, A R
- Héon, E
- Lotery, A J
- Vandenburgh, K
- Casavant, T L
- Oh, K T
- Beck, G
- Fishman, G A
- Lam, B L
- Levin, A
- Heckenlively, J R
- Jacobson, S G
- Weleber, R G
- Sheffield, V C
- Stone, E M
Producer: 20010510
In:
Investigative ophthalmology & visual science vol. 42
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500.
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A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. [electronic resource] by
- Stone, E M
- Lotery, A J
- Munier, F L
- Héon, E
- Piguet, B
- Guymer, R H
- Vandenburgh, K
- Cousin, P
- Nishimura, D
- Swiderski, R E
- Silvestri, G
- Mackey, D A
- Hageman, G S
- Bird, A C
- Sheffield, V C
- Schorderet, D F
Producer: 19990629
In:
Nature genetics vol. 22
Availability: No items available.
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