-
1
-
-
0030875991
-
Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population
-
AN Akarsu U Saatci S Ozen A Bakkaloglu N Besbas S Mansoor Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population J Med Genet 34 1997 573 578
-
(1997)
J Med Genet
, vol.34
, pp. 573-578
-
-
Akarsu, AN1
Saatci, U2
Ozen, S3
Bakkaloglu, A4
Besbas, N5
Mansoor, S6
-
2
-
-
18244429610
-
Mutation and haplotype studies in familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population
-
I Aksentijevich Y Torosyan J Samuels M Centola E Pras JJ Chae C Oddoux Mutation and haplotype studies in familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population Am J Hum Genet 64 1999 949 962 (in this issue)
-
(1999)
Am J Hum Genet
, vol.64
, pp. 949-962
-
-
Aksentijevich, I1
Torosyan, Y2
Samuels, J3
Centola, M4
Pras, E5
Chae, JJ6
Oddoux, C7
-
4
-
-
0032561502
-
A physical map of 30,000 human genes
-
P Deloukas GD Schuler G Gyapay EM Beasley C Soderlund P Rodriguez-Tomé L Hui A physical map of 30,000 human genes Science 282 1998 744 746
-
(1998)
Science
, vol.282
, pp. 744-746
-
-
Deloukas, P1
Schuler, GD2
Gyapay, G3
Beasley, EM4
Soderlund, C5
Rodriguez-Tomé, P6
Hui, L7
-
5
-
-
16944365196
-
A candidate gene for familial Mediterranean fever
-
French FMF Consortium A candidate gene for familial Mediterranean fever Nat Genet 17 1997 25 31
-
(1997)
Nat Genet
, vol.17
, pp. 25-31
-
-
French FMF Consortium1
-
7
-
-
0030745449
-
Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever
-
International FMF Consortium, The Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever Cell 90 1997 797 807
-
(1997)
Cell
, vol.90
, pp. 797-807
-
-
International FMF Consortium, The,1
-
12
-
-
0029816014
-
Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema
-
E Verpy M Biasotto M Brai G Misiano T Meo M Tosi Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema Am J Hum Genet 59 1996 308 319
-
(1996)
Am J Hum Genet
, vol.59
, pp. 308-319
-
-
Verpy, E1
Biasotto, M2
Brai, M3
Misiano, G4
Meo, T5
Tosi, M6
-
13
-
-
0027278997
-
Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation
-
SD Wilton RD Johnsen JR Pedretti NG Laing Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation Am J Med Genet 46 1993 563 569
-
(1993)
Am J Med Genet
, vol.46
, pp. 563-569
-
-
Wilton, SD1
Johnsen, RD2
Pedretti, JR3
Laing, NG4
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