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Results 21-23 of 23 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
1997
A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groups
Balow Jnr., J.
;
Shelton, D.
;
Orsborn, A.
;
Mangelsdorf, M.
;
Aksentijevich, I.
;
Blake, T.
;
Sood, R.
;
Gardner, D.
;
Liu, R.
;
Pras, E.
;
Levy, E.
;
Centola, M.
;
Deng, Z.
;
Zaks, N.
;
Wood, G.
;
Chen, X.
;
Richards, N.
;
Shohat, M.
;
Livneh, A.
;
Pras, M.
;
et al.
1997
Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor family
Somers, G.
;
Hammet, F.
;
Woollatt, E.
;
Richards, R.
;
Southey, M.
;
Venter, D.
Discover
Author
9
Mulley, J.
7
Callen, D.
5
Eyre, H.
5
Gedeon, A.
3
Donnelly, A.
3
Sutherland, G.
2
Aksentijevich, I.
2
Baker, E.
2
Blake, T.
2
Centola, M.
.
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Subject
23
Humans
17
Male
13
Female
9
Chromosomes, Human, Pair 16
9
Genetic Linkage
8
Genetic Markers
8
X Chromosome
7
Molecular Sequence Data
6
Intellectual Disability
6
Pedigree
.
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Date issued
1
2010 - 2017
22
1996 - 1999