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Showing results 1 to 2 of 2
Title
Author(s)
Issue Date
Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus
Journal:
American Journal of Human Genetics
Hamosh, A
King, TM
Rosenstein, BJ
Corey, M
Levison, H
Durie, P
Tsui , LC
Mcintosh, I
Keston, M
Brock, DJH
Macek Jr, M
Zemkova, D
Krasnicanova, H
Vavrova, V
Macek Sr, M
Golder, N
Schwarz, MJ
Super, M
Watson, EK
1992
Unusual segregation of cystic fibrosis alleles [6]
Journal:
Nature
Kitzis, A
Chomel, JC
Haliassos, A
Tesson, L
Kaplan, JC
Feingold, J
Giraud, G
Labbe, A
Dastugue, B
Dumur, V
Farriaux, JP
Roussel, P
Ferrec, C
Vidaud, M
Goossens, M
Bozon, D
Auvinet, M
Chambon, V
Andre, J
Lissens, W
Bonduelle, M
Liebaers, I
Cochaux, P
Vassart, G
Willems, P
DuckworthRaysiecki, G
Kerem, BS
Tsui, LC
Ray, PN
Krawczak, M
Schmidtke, J
Novelli, G
Dallapiccola, B
Gasparni, G
Pignatti, PP
Seia, M
Ferrari, M
Devoto, M
Romeo, G
Schwarz, M
Super, M
Ivinson, A
Read, AP
Meredith, L
Curtis, A
Williamson, R
Beaudet, AL
Feldman, GL
O'Brien, WE
Bowcock, AM
CavalliSforza, LL
Gilbert, F
Braman, J
King, MC
1988