|
🐜
|
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.
12 auth.
S. Baker,
E. Fearon,
J. Nigro,
S. Hamilton,
A. C. Preisinger,
J. Jessup,
...
P. Vantuinen,
D. Ledbetter,
D. Barker,
Y. Nakamura,
Raymond White,
B. Vogelstein
|
11 |
1989 |
11
🐜
|
|
🐜
|
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
12 auth.
J. Lupski,
R. M. Oca-Luna,
S. Slaugenhaupt,
L. Pentao,
V. Guzzetta,
B. Trask,
...
O. Saucedo-Cárdenas,
D. Barker,
J. Killian,
Carlos A. Garcia,
A. Chakravarti,
P. Patel
|
10 |
1991 |
10
🐜
|
|
🐜
|
A genetic linkage map of the human genome
33 auth.
H. Donis-Keller,
P. Green,
C. Helms,
S. Cartinhour,
B. Weiffenbach,
K. Stephens,
T. Keith,
D. Bowden,
Douglas R. Smith,
E. Lander,
D. Botstein,
G. Akots,
K. Rediker,
T. Gravius,
V. Brown,
...
Marcia B. Rising,
C. Parker,
J. A. Powers,
D. Watt,
E. Kauffman,
A. Bricker,
P. Phipps,
Hans Muller-Kahle,
T. R. Fulton,
S. Ng,
J. Schumm,
J. Braman,
R. Knowlton,
D. Barker,
S. Crooks,
S. Lincoln,
M. Daly,
Jeff Abrahamson
|
9 |
1987 |
9
🐜
|
|
🦁
|
Identification of mutations in the COL4A5 collagen gene in Alport syndrome.
10 auth.
D. Barker,
S. L. Hostikka,
Jing Zhou,
L. Chow,
A. Oliphant,
S. Gerken,
...
M. Gregory,
M. Skolnick,
C. Atkin,
K. Tryggvason
|
9 |
1990 |
9
🦁
|
|
🦁
|
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.
20 auth.
D. Barker,
E. Wright,
K. Nguyen,
L. Cannon,
P. Fain,
D. Goldgar,
D. Bishop,
J. Carey,
B. Baty,
J. Kivlin,
...
H. Willard,
J. Waye,
G. M. Greig,
L. Leinwand,
Y. Nakamura,
P. O'Connell,
M. Leppert,
J. Lalouel,
Raymond White,
M. Skolnick
|
9 |
1987 |
9
🦁
|
|
🐜
|
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
11 auth.
P. Raeymaekers,
V. Timmerman,
E. Nelis,
P. Jonghe,
J. E. Hoogenduk,
F. Baas,
...
D. Barker,
J. Martin,
M. Visser,
P. Bolhuis,
C. Broeckhoven
|
9 |
1991 |
9
🐜
|
|
🦁
|
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA
D. Barker,
Mireille Schafer,
Raymond White
|
9 |
1984 |
9
🦁
|
|
🦁
|
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA
D. Barker,
Mireille Schafer,
Raymond White
|
9 |
1984 |
9
🦁
|
|
🐜
|
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7
11 auth.
R. Knowlton,
O. Cohen-Haguenauer,
N. Cong,
J. Frézal,
V. Brown,
D. Barker,
...
J. Braman,
J. Schumm,
L. Tsui,
M. Buchwald,
H. Donis-Keller
|
8 |
1985 |
8
🐜
|
|
🐜
|
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
15 auth.
K. Heath,
Á. Campos-Barros,
A. Toren,
G. Rozenfeld-Granot,
L. Carlsson,
J. Savige,
J. Denison,
M. Gregory,
J. White,
D. Barker,
...
A. Greinacher,
C. Epstein,
M. Glucksman,
M. Glucksman,
J. Martignetti
|
8 |
2001 |
8
🐜
|
|
🐜
|
Construction of linkage maps with DNA markers for human chromosomes
9 auth.
Raymond White,
M. Leppert,
D. Timothy Bishop,
D. Barker,
J. Berkowitz,
Candace Brown,
...
P. Callahan,
T. Holm,
L. Jerominski
|
8 |
1985 |
8
🐜
|
|
🐜
|
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17
10 auth.
J. Vance,
G. Nicholson,
L. Yamaoka,
J. Stajich,
C. Stewart,
M. Speer,
...
W. Hung,
A. Roses,
D. Barker,
M. Pericak-Vance
|
7 |
1989 |
7
🐜
|
|
🐜
|
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.
7 auth.
D. Page,
B. de Martinville,
D. Barker,
A. Wyman,
R. White,
U. Francke,
...
D. Botstein
|
7 |
1982 |
7
🐜
|
