Results
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31401.
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31402.
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31403.
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Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts. [electronic resource] by
- Hilal, Latifa
- Nandrot, Emeline
- Belmekki, Mohamed
- Chefchaouni, Mohamed
- El Bacha, Siham
- Benazzouz, Bouchra
- Hajaji, Yassir
- Gribouval, Olivier
- Dufier, Jean
- Abitbol, Marc
- Berraho, Amina
Producer: 20030418
In:
Ophthalmic genetics vol. 23
Availability: No items available.
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31404.
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Chromosomal abnormalities and microsatellite instability in sporadic endometrial cancer. [electronic resource] by
- Muresu, R
- Sini, M C
- Cossu, A
- Tore, S
- Baldinu, P
- Manca, A
- Pisano, M
- Loddo, C
- Dessole, S
- Pintus, A
- Tanda, F
- Palmieri, G
Producer: 20021112
In:
European journal of cancer (Oxford, England : 1990) vol. 38
Availability: No items available.
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31405.
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Prevalence and prognostic role of microsatellite instability in patients with rectal carcinoma. [electronic resource] by
- Colombino, M
- Cossu, A
- Manca, A
- Dedola, M F
- Giordano, M
- Scintu, F
- Curci, A
- Avallone, A
- Comella, G
- Amoruso, M
- Margari, A
- Bonomo, G M
- Castriota, M
- Tanda, F
- Palmieri, G
Producer: 20021204
In:
Annals of oncology : official journal of the European Society for Medical Oncology vol. 13
Availability: No items available.
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31406.
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Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts. [electronic resource] by
- Nandrot, E
- Slingsby, C
- Basak, A
- Cherif-Chefchaouni, M
- Benazzouz, B
- Hajaji, Y
- Boutayeb, S
- Gribouval, O
- Arbogast, L
- Berraho, A
- Abitbol, M
- Hilal, L
Producer: 20030417
In:
Journal of medical genetics vol. 40
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31407.
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31408.
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An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5. [electronic resource] by
- Michaelides, Michel
- Johnson, Samantha
- Tekriwal, Alok K
- Holder, Graham E
- Bellmann, Caren
- Kinning, Esther
- Woodruff, Geoffrey
- Trembath, Richard C
- Hunt, David M
- Moore, Anthony T
Producer: 20030519
In:
Investigative ophthalmology & visual science vol. 44
Availability: No items available.
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31409.
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Association studies between microsatellite markers within the gene encoding human 11beta-hydroxysteroid dehydrogenase type 1 and body mass index, waist to hip ratio, and glucocorticoid metabolism. [electronic resource] by
- Draper, N
- Echwald, S M
- Lavery, G G
- Walker, E A
- Fraser, R
- Davies, E
- Sørensen, T I A
- Astrup, A
- Adamski, J
- Hewison, M
- Connell, J M
- Pedersen, O
- Stewart, P M
Producer: 20021209
In:
The Journal of clinical endocrinology and metabolism vol. 87
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31410.
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31411.
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CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours. [electronic resource] by
- Sodha, N
- Bullock, S
- Taylor, R
- Mitchell, G
- Guertl-Lackner, B
- Williams, R D
- Bevan, S
- Bishop, K
- McGuire, S
- Houlston, R S
- Eeles, R A
Producer: 20030107
In:
British journal of cancer vol. 87
Availability: No items available.
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31412.
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31413.
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Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin. [electronic resource] by
- Moreira, E S
- Wiltshire, T J
- Faulkner, G
- Nilforoushan, A
- Vainzof, M
- Suzuki, O T
- Valle, G
- Reeves, R
- Zatz, M
- Passos-Bueno, M R
- Jenne, D E
Producer: 20000228
In:
Nature genetics vol. 24
Availability: No items available.
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31414.
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31415.
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31416.
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31417.
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31418.
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31419.
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Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. [electronic resource] by
- Hirschhorn, J N
- Lindgren, C M
- Daly, M J
- Kirby, A
- Schaffner, S F
- Burtt, N P
- Altshuler, D
- Parker, A
- Rioux, J D
- Platko, J
- Gaudet, D
- Hudson, T J
- Groop, L C
- Lander, E S
Producer: 20010802
In:
American journal of human genetics vol. 69
Availability: No items available.
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31420.
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