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Results 1-10 of 16 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1998
Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3
Centola, M.
;
Chen, X.
;
Sood, R.
;
Deng, Z.
;
Aksentijevich, I.
;
Blake, T.
;
Ricke, D.
;
Chen, X.
;
Wood, G.
;
Zaks, N.
;
Richards, N.
;
Krizman, D.
;
Mansfield, E.
;
Apostolou, S.
;
Liu, J.
;
Shafran, N.
;
Vedula, A.
;
Hamon, M.
;
Cercek, A.
;
Kahan, T.
;
et al.
1998
Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13.
Nomiyama, H.
;
Imai, T.
;
Kusuda, J.
;
Miura, R.
;
Callen, D.
;
Yoshie, O.
1998
Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2y: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.
Schollen, E.
;
Pardon, E.
;
Heykants, L.
;
Renard, J.P.
;
Doggett, N.
;
Callen, D.
;
Cassiman, J.J.
;
Matthijs, G.
1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3
Cleton-Jansen, A.M.
;
Moerland, E.
;
Pronk, J.
;
Van Berkel, C.
;
Apostolou, S.
;
Crawford, J.
;
Savoia, A.
;
Auerbach, A.
;
Callen, D.
;
Cornelisse, C.
1997
Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever
Aksentijevich, I.
;
Centola, M.
;
Deng, Z.
;
Sood, R.
;
Balow, J.
;
Wood, G.
;
Zaks, N.
;
Mansfield, E.
;
Chen, X.
;
Eisenberg, S.
;
Vedula, A.
;
Shafran, N.
;
Raben, N.
;
Pras, E.
;
Pras, M.
;
Kastner, D.
;
Blake, T.
;
Baxevanis, A.
;
Robbins, C.
;
Krizman, D.
;
et al.
1997
Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2
Horwitz, M.
;
Benson, K.
;
Li, F.Q.
;
Wolff, J.
;
Leppert, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Yu, S.
;
Hewett, D.
;
Richards, R.
;
Raskind, W.
1998
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
Cavanaugh, J.
;
Callen, D.
;
Wilson, S.
;
Stanford, P.
;
Sraml, M.
;
Gorska, M.
;
Crawford, J.
;
Whitmore, S.
;
Shlegel, C.
;
Foote, S.
;
Kohonen-Corish, M.
;
Pavli, P.
1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Settasatian, C.
;
Whitmore, S.
;
Crawford, J.
;
Bilton, R.
;
Cleton-Jansen, A.M.
;
Sutherland, G.
;
Callen, D.
1997
Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13
Nomiyama, H.
;
Imai, T.
;
Kusuda, J.
;
Miura, R.
;
Callen, D.
;
Yoshie, O.
1998
Localisation of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.
Kremmidiotis, G.
;
Baker, E.
;
Crawford, J.
;
Eyre, H.
;
Nahmias, J.
;
Callen, D.
Discover
Author
11
Callen, D.
6
Crawford, J.
4
Aksentijevich, I.
4
Blake, T.
4
Centola, M.
4
Chen, X.
4
Cleton-Jansen, A.M.
4
Deng, Z.
4
Doggett, N.
4
et al.
.
next >
Subject
16
Humans
9
Chromosome Mapping
7
Female
7
Molecular Sequence Data
5
Cloning, Molecular
4
Base Sequence
4
Breast Neoplasms
4
Familial Mediterranean Fever
4
Male
3
Amino Acid Sequence
.
next >
Date issued
3
1999
8
1998
5
1997