R N Mackinnon
Overview
Explore the profile of R N Mackinnon including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
11
Citations
185
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Mackinnon R, Campbell L
Cytogenet Genome Res
. 2008 Feb;
119(3-4):211-20.
PMID: 18253031
FISH analysis of 41 previously karyotyped cases of MDS and AML with apparent monosomy of chromosome 20 revealed a variety of dicentric abnormalities involving chromosome 20. These usually, but not...
2.
Daniels R, Thomas N, Mackinnon R, Lehner T, Ott J, Flint T, et al.
Genomics
. 1992 Feb;
12(2):335-9.
PMID: 1346777
Linkage data between four markers on chromosome 5 confirm and extend our previous studies that localized the mutation in spinal muscular atrophy to 5q11.2-q13.3. Localization of D5S6 by in situ...
3.
Rosenthal A, Mackinnon R, Jones D
Nucleic Acids Res
. 1991 Oct;
19(19):5395-401.
PMID: 1923824
Microdissection has proved to be a powerful tool in the construction of libraries from specific chromosome segments (11) which are poorly covered by existing RFLP markers. Microclones also represent starting...
4.
Hirst M, Rack K, Nakahori Y, Roche A, Bell M, Flynn G, et al.
Nucleic Acids Res
. 1991 Jun;
19(12):3283-8.
PMID: 2062644
The fragile X syndrome is a common cause of mental retardation and is associated with a fragile site at Xq27.3 (FRAXA). Recently, evidence has been presented for the role of...
5.
Hirst M, Roche A, Flint T, Mackinnon R, Bassett J, Nakahori Y, et al.
Genomics
. 1991 May;
10(1):243-9.
PMID: 2045104
We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the fragile site at Xq27.3. So far, no microdissection markers derived from Xq28...
6.
Bell M, Hirst M, Nakahori Y, Mackinnon R, Roche A, Flint T, et al.
Cell
. 1991 Feb;
64(4):861-6.
PMID: 1997211
The most common genetic cause of mental retardation after Down's syndrome, the fragile X syndrome, is associated with the occurrence of a fragile site at Xq27.3. This X-linked disease is...
7.
Hirst M, Bell M, Mackinnon R, Watson J, Callen D, Sutherland G, et al.
Am J Med Genet
. 1991 Feb;
38(2-3):354-6.
PMID: 1673311
We have localized the gene encoding a cerebellar degeneration related (CDR) protein to a region proximal to the fragile site close to DXS98 and DXS105. This gene is polymorphic with...
8.
Mackinnon P, Powell B, ROGERS G, Baker E, Mackinnon R, Hyland V, et al.
Mamm Genome
. 1991 Jan;
1(1):53-6.
PMID: 1724400
A human hair cuticle ultrahigh-sulphur keratin Q (UHSK) gene (KRN1) has been mapped by Southern analysis of a somatic cell hybrid panel and by in situ hybridization. A probe containing...
9.
Mackinnon R, Hirst M, Bell M, Watson J, Claussen U, Ludecke H, et al.
Am J Hum Genet
. 1990 Aug;
47(2):181-6.
PMID: 2378345
We have microdissected and cloned the region around the fragile site at Xq27.3 on the human X chromosome. All of the clones tested map to the Xq27-Xq28 region, and detailed...
10.
Hyland V, Suthers G, Friend K, Mackinnon R, Callen D, Breuning M, et al.
Hum Genet
. 1990 Feb;
84(3):286-8.
PMID: 1968038
The polymorphic DNA probe VK5B (D16S94) was mapped by genetic linkage in families from the Centre d'Etude de Polymorphisme Humain (CEPH) as being in the same interval as the autosomal...